FT CDS join(5721..5921,6225..6368,6657..6813,6945..6972, FT 7581..7689,7772..7864,7968..8031,8450..8548, FT 8788..8891,9538..9676,10095..10213,10338..10487, FT 10772..10942,11547..11856,12128..12195, FT 12570..12657,13352..13469,13615..13738, FT 14015..14151,14408..14663,15283..15525, FT 15709..15885,17101..17246,18377..18467, FT 19193..19582,19818..19944,20132..20250, FT 21021..21217,21741..21924,22109..22274, FT 22435..22559,23115..23423,23595..23798, FT 23921..24046,24157..24432,25327..25422, FT 25536..25670,26558..26575) FT /note=MYH7 FT mutation 5748..5750 FT /label="Gly10del" FT /note="Gly10del, del GGG" FT mutation 5797 FT /label="A26V" FT /note="Ala26Val, C>T" FT mutation 5835 FT /label="V39M" FT /note="Val39Met, G>A" FT mutation 5895 FT /label="V59I" FT /note="Val59Ile, G>A" FT mutation 6366 FT /label="Y115H" FT /note="Tyr115His, T>C" FT mutation 6682 FT /label="T124I" FT /note="Thr124Ile, C>T" FT mutation 6738 FT /label="R143W" FT /note="Arg143Trp, C>T" FT mutation 6739 FT /label="R143Q" FT /note="Arg143Gln, G>A" FT mutation 6749 FT /label="K146N" FT /note="Lys146Asn, G>T" FT mutation 6796 FT /label="Y162C" FT /note="Tyr162Cys, A>G" FT mutation 7606 FT /label="V186L" FT /note="Val186Leu, G>C" FT mutation 7611 FT /label="N187K" FT /note="Asn187Lys, C>G" FT mutation 7613 FT /label="T188N" FT /note="Thr188Asn, C>A" FT mutation 7619 FT /label="R190T" FT /note="Arg190Thr, G>C" FT mutation 7636 FT /label="A196T" FT /note="Ala196Thr, G>A" FT mutation 7652 FT /label="Ile201Thr" FT /note="Ile201Thr, T>C" FT mutation 7661 FT /label="R204H" FT /note="Arg204His, G>A" FT mutation 7669 FT /label="K207Q" FT /note="Lys207Gln, A>C" FT mutation 7682 FT /label="P211L" FT /note="Pro211Leu, C>T" FT mutation 7796 FT /label="Q222K" FT /note="Gln222Lys, C>A" FT mutation 7799 FT /label="A223T" FT /note="Ala223Thr, G>A" FT mutation 7811 FT /label="L227V" FT /note="Leu227Val, C>G" FT mutation 7827 FT /label="N232S" FT /note="Asn232Ser, A>G" FT mutation 7863..7864 FT /label="F244L" FT /note="Phe244Leu, unspecified" FT mutation 7971 FT /label="K246Q" FT /note="Lys246Gln, A>C" FT mutation 7981 FT /label="R249Q" FT /note="Arg249Gln, G>A" FT mutation 8002 FT /label="G256E" FT /note="Gly256Glu, G>A" FT mutation 8023 FT /label="I263T" FT /note="Ile263Thr, T>C" FT mutation 8024 FT /label="I263M" FT /note="Ile263Met, A>G" FT mutation 8827 FT /label="F312C" FT /note="Phe312Cys, T>G" FT mutation 8850 FT /label="V320M" FT /note="Val320Met, G>A" FT mutation 8868 FT /label="A326P" FT /note="Ala326Pro, G>C" FT mutation 8875 FT /label="E328G" FT /note="Glu328Gly, A>G" FT mutation 9584 FT /label="M349T" FT /note="Met349Thr, T>C" FT mutation 9589 FT /label="K351E" FT /note="Lys351Glu, A>G" FT mutation 9601 FT /label="A355T" FT /note="Ala355Thr, G>A" FT mutation 10105 FT /label="K383N" FT /note="Lys383Asn, G>T" FT mutation 10110 FT /label="A385V" FT /note="Ala385Val, C>T" FT mutation 10124..10126 FT /label="L390V" FT /note="Leu390Val, del CTG, ins GTT" FT mutation 10133 FT /label="Ala393Thr" FT /note="Ala393Thr, G>A" FT mutation 10163 FT /label="R403W" FT /note="Arg403Trp, C>T" FT mutation 10164 FT /label="R403L" FT /note="Arg403Leu, G>T" FT mutation 10164 FT /label="R403Q" FT /note="Arg403Gln, G>A" FT mutation 10166 FT /label="V404M" FT /note="Val404Met, G>A" FT mutation 10166 FT /label="V404L" FT /note="Val404Leu, G>C" FT mutation 10172 FT /label="V406M" FT /note="Val406Met, G>A" FT mutation 10176 FT /label="G407V" FT /note="Gly407Val, G>T" FT mutation 10187 FT /label="V411I" FT /note="Val411Ile, G>A" FT mutation 10191 FT /label="Thr412Asn" FT /note="Thr412Asn, C>A" FT mutation 10353 FT /label="Gly425Arg" FT /note="Gly425Arg, G>A" FT mutation 10363 FT /label="A428V" FT /note="Ala428Val, C>T" FT mutation 10369 FT /label="A430E" FT /note="Ala430Glu, A>C" FT mutation 10384 FT /label="M435T" FT /note="Met435Thr, T>C" FT mutation 10398 FT /label="V440M" FT /note="Val440Met, G>A" FT mutation 10405 FT /label="R442H" FT /note="Arg442His, G>A" FT mutation 10408 FT /label="I443T" FT /note="Ile443Thr, T>C" FT mutation 10428 FT /label="K450Q" FT /note="Lys450Glu, A>G" FT mutation 10429 FT /label="Lys450Thr" FT /note="Lys450Thr, A>C" FT mutation 10437 FT /label="R453C" FT /note="Arg453Cys, C>T" FT mutation 10438 FT /label="R453H" FT /note="Arg453His, G>A" FT mutation 10438 FT /label="R453L" FT /note="Arg453Leu, G>T" FT mutation 10800 FT /label="N479S" FT /note="Asn479Ser, A>G" FT mutation 10811 FT /label="E483K" FT /note="Glu483Lys, G>A" FT mutation 10855 FT /label="E497D" FT /note="Glu497Asp, G>T" FT mutation 10859 FT /label="E499K" FT /note="Glu499Lys, G>A" FT mutation 10866 FT /label="Tyr501Cys" FT /note="Tyr501Cys, A>G" FT mutation 10895 FT /label="Ile511Phe" FT /note="Ile511Phe, A>T" FT mutation 10896 FT /label="I511T" FT /note="Ile511Thr, T>C" FT mutation 10902 FT /label="F513C" FT /note="Phe513Cys, T>G" FT mutation 10908 FT /label="M515R" FT /note="Met515Arg, T>G" FT mutation 10913 FT /label="L517M" FT /note="Leu517Met, C>A" FT mutation 11562 FT /label="S532P" FT /note="Ser532Pro, T>C" FT mutation 11617 FT /label="Ala550Val" FT /note="Ala550Val, C>T" FT mutation 11695 FT /label="H576R" FT /note="His576Arg, A>G" FT mutation 11718 FT /label="G584S" FT /note="Gly584Ser, G>A" FT mutation 11718 FT /label="G584R" FT /note="Gly584Arg, G>C" FT mutation 11728 FT /label="D587V" FT /note="Asp587Val, A>T" FT mutation 11752 FT /label="Q595R" FT /note="Gln595Arg, A>G" FT mutation 11769 FT /label="L601V" FT /note="Leu601Val, C>G" FT mutation 11773 FT /label="N602S" FT /note="Asn602Ser, A>G" FT mutation 11784 FT /label="V606M" FT /note="Val606Met, G>A" FT mutation 11784 FT /label="V606L" FT /note="Val606Leu, G>C" FT mutation 11801 FT /label="K611N" FT /note="Lys611Asn, G>T" FT mutation 11813 FT /label="K615N" FT /note="Lys615Asn, G>C" FT mutation 11838 FT /label="Y624N" FT /note="Tyr624Asn, T>A" FT mutation 12164 FT /label="S642L" FT /note="Ser642Leu, C>T" FT mutation 12193 FT /label="R652G" FT /note="Arg652Gly, A>G" FT mutation 12590 FT /label="M659I" FT /note="Met659Ile, G>A" FT mutation 12600 FT /label="R663C" FT /note="Arg663Cys, C>T" FT mutation 12601 FT /label="R663H" FT /note="Arg663His, G>A" FT mutation 12624 FT /label="R671C" FT /note="Arg671Cys, C>T" FT mutation 12776 FT /label="R1712Q" FT /note="Arg1712Gln, G>A" FT mutation 13387 FT /label="R694C" FT /note="Arg694Cys, C>T" FT mutation 13388 FT /label="R694H" FT /note="Arg694His, G>A" FT mutation 13394 FT /label="N696S" FT /note="Asn696Ser, A>G" FT mutation 13400 FT /label="V698A" FT /note="Val698Ala, T>C" FT mutation 13442 FT /label="R712L" FT /note="Arg712Leu, G>T" FT mutation 13453 FT /label="G716R" FT /note="Gly716Arg, G>A" FT mutation 13462 FT /label="R719W" FT /note="Arg719Trp, C>T" FT mutation 13463 FT /label="R719P" FT /note="Arg719Pro, G>C" FT mutation 13463 FT /label="R719Q" FT /note="Arg719Gln, G>A" FT mutation 13619 FT /label="R723C" FT /note="Arg723Cys, C>T" FT mutation 13619 FT /label="R723G" FT /note="Arg723Gly, C>G" FT mutation 13635 FT /label="A728V" FT /note="Ala728Val, C>T" FT mutation 13644 FT /label="P731L" FT /note="Pro731Leu, C>T" FT mutation 13650 FT /label="G733E" FT /note="Gly733Glu, G>A" FT mutation 13652 FT /label="Q734E" FT /note="Gln734Glu, C>G" FT mutation 13653 FT /label="Gln734Pro" FT /note="Gln734Pro, A>C" FT mutation 13658 FT /label="I736V" FT /note="Ile736Val, A>G" FT mutation 13659 FT /label="I736T" FT /note="Ile736Thr, T>C" FT mutation 13660 FT /label="I736M" FT /note="Ile736Met, T>G" FT mutation 13673 FT /label="G741W" FT /note="Gly741Trp, G>T" FT mutation 13673 FT /label="G741R" FT /note="Gly741Arg, G>A" FT mutation 13673 FT /label="G741R" FT /note="Gly741Arg, G>C" FT mutation 13674 FT /label="G741A" FT /note="Gly741Ala, G>C" FT mutation 13677 FT /label="A742E" FT /note="Ala742Glu, C>A" FT mutation 14020 FT /label="F764L" FT /note="Phe764Leu, C>G" FT mutation 14026 FT /label="Lys766Asn" FT /note="Lys766Asn, uncertain" FT mutation 14030 FT /label="G768R" FT /note="Gly768Arg, G>C" FT mutation 14049 FT /label="E774V" FT /note="Glu774Val, A>T" FT mutation 14061 FT /label="D778V" FT /note="Asp778Val, A>T" FT mutation 14061 FT /label="D778G" FT /note="Asp778Gly, A>G" FT mutation 14062 FT /label="D778E" FT /note="Asp778Glu, C>G" FT mutation 14063 FT /label="E779X" FT /note="Glu779ter, G>T" FT mutation 14071..14073 FT /label="Ser782Asp" FT /note="Ser782Asp, del GAG, ins AGA" FT mutation 14073 FT /label="S782N" FT /note="Ser782Asn, G>A" FT mutation 14088 FT /label="R787H" FT /note="Arg787His, G>A" FT mutation 14114 FT /label="L796F" FT /note="Leu796Phe, C>T" FT mutation 14117 FT /label="A797T" FT /note="Ala797Thr, G>A" FT mutation 14117 FT /label="Ala797Pro" FT /note="Ala797Pro, G>C" FT mutation 14448 FT /label="M822V" FT /note="Met822Val, A>G" FT mutation 14449 FT /label="Met822Thr" FT /note="Met822Thr, T>C" FT mutation 14452 FT /label="Gly823Glu" FT /note="Gly823Glu, G>A" FT mutation 14454 FT /label="V824I" FT /note="Val824Ile, G>A" FT mutation 14520 FT /label="E846Q" FT /note="Glu846Gln, G>C" FT mutation 14520 FT /label="E846K" FT /note="Glu846Lys, G>A" FT mutation 14523..14525 FT /label="K847del" FT /note="Lys847del, AAG>del" FT mutation 14539 FT /label="M852T" FT /note="Met852Thr, T>C" FT mutation 14556 FT /label="R858C" FT /note="Arg858Cys, C>T" FT mutation 14557 FT /label="Arg858His" FT /note="Arg858His, G>A" FT mutation 14581 FT /label="S866Y" FT /note="Ser866Tyr, C>A" FT mutation 14589 FT /label="R869G" FT /note="Arg869Gly, C>G" FT mutation 14589 FT /label="R869C" FT /note="Arg869Cys, C>T" FT mutation 14590 FT /label="R869H" FT /note="Arg869His, G>A" FT mutation 14592 FT /label="R870C" FT /note="Arg870Cys, C>T" FT mutation 14593 FT /label="R870H" FT /note="Arg870His, G>A" FT mutation 14593 FT /label="R870L" FT /note="Arg870Leu, G>T" FT mutation 14614 FT /label="M877K" FT /note="Met877Lys, T>A" FT mutation 14631..14633 FT /label="E883del" FT /note="Glu883del, GAG>del" FT mutation 14650 FT /label="L889H" FT /note="Leu889His, T>A" FT mutation 15284 FT /label="E894G" FT /note="Glu894Gly, A>G" FT mutation 15305 FT /label="Ala901Gly" FT /note="Ala901Gly, C>G" FT mutation 15317 FT /label="C905F" FT /note="Cys905Phe, G>T" FT mutation 15320 FT /label="D906G" FT /note="Asp906Gly, A>G" FT mutation 15325 FT /label="L908V" FT /note="Leu908Val, C>G" FT mutation 15328 FT /label="Ile909Val" FT /note="Ile909Val, A>G" FT mutation 15364 FT /label="E921K" FT /note="Glu921Lys, G>A" FT mutation 15373 FT /label="E924K" FT /note="Glu924Lys, G>A" FT mutation 15373 FT /label="E924Q" FT /note="Glu924Gln, G>C" FT mutation 15380 FT /label="E927del" FT /note="Glu927del, del GGA" FT mutation 15382 FT /label="E927K" FT /note="Glu927Lys, G>A" FT mutation 15385 FT /label="D928N" FT /note="Asp928Asn, G>A" FT mutation 15391 FT /label="E930K" FT /note="Glu930Lys, G>A" FT mutation 15391..15393 FT /label="E930del" FT /note="Glu930del, del GAG" FT mutation 15394 FT /label="E931K" FT /note="Glu931Lys, G>A" FT mutation 15406 FT /label="E935K" FT /note="Glu935Lys, G>A" FT mutation 15448 FT /label="E949K" FT /note="Glu949Lys, G>A" FT mutation 15460 FT /label="D953H" FT /note="Asp953His, G>C" FT mutation 15485 FT /label="L961R" FT /note="Leu961Arg, T>G" FT mutation 15842 FT /label="Thr1019Asn" FT /note="Thr1019Asn, C>A" FT mutation 17159 FT /label="Arg1053Gln" FT /note="Arg1053Gln, G>A" FT mutation 17170 FT /label="G1057S" FT /note="Gly1057Ser, G>A" FT mutation 18432 FT /label="G1101S" FT /note="Gly1101Ser, G>A" FT mutation 19260 FT /label="L1135R" FT /note="Leu1135Arg, T>G" FT mutation 19433 FT /label="Arg1193Ser" FT /note="Arg1193Ser, C>A" FT mutation 19508 FT /label="E1218Q" FT /note="Glu1218Gln, G>C" FT mutation 21029 FT /label="N1327K" FT /note="Asn1327Lys, " FT mutation 21048 FT /label="Gln1334ter" FT /note="Gln1334ter, C>T" FT mutation 21114 FT /label="E1356K" FT /note="Glu1356Lys, G>A" FT mutation 21178 FT /label="E1377M" FT /note="Glu1377Met, C>T" FT mutation 21183 FT /label="A1379T" FT /note="Ala1379Thr, G>A" FT mutation 21192 FT /label="R1382W" FT /note="Arg1382Trp, C>T" FT mutation 21829 FT /label="R1420W" FT /note="Arg1420Trp, C>T" FT mutation 21847 FT /label="Glu1426Lys" FT /note="Glu1426Lys, G>A" FT mutation 22115 FT /label="Ala1454Thr" FT /note="Ala1454Thr, G>A" FT mutation 22132 FT /label="K1459N" FT /note="Lys1459Asn, " FT mutation 22178 FT /label="Arg1475Cys" FT /note="Arg1475Cys, C>T" FT mutation 22227 FT /label="Ser1491Cys" FT /note="Ser1491Cys, C>G" FT mutation 22253 FT /label="Arg1500Trp" FT /note="Arg1500Trp, C>T" FT mutation 22452 FT /label="T1513S" FT /note="Thr1513Ser, A>T" FT mutation 23133 FT /label="E1555K" FT /note="Glu1555Lys, G>A" FT mutation 23370 FT /label="Arg1634Cys" FT /note="Arg1634Cys, C>T" FT mutation 23712 FT /label="V1691M" FT /note="Val1691Met, G>A" FT mutation 23775 FT /label="R1712W" FT /note="Arg1712Trp, C>T" FT mutation 24020 FT /label="E1753K" FT /note="Glu1753Lys, G>A" FT mutation 24175 FT /label="E1768K" FT /note="Glu1768Lys, G>A" FT mutation 24199 FT /label="S1776G" FT /note="Ser1776Gly, A>G" FT mutation 24202 FT /label="A1777T" FT /note="Ala1777Thr, G>A" FT mutation 24406 FT /label="R1845W" FT /note="Arg1845Trp, C>T" FT mutation 25582 FT /label="His1901Leu" FT /note="His1901Leu, A>T" FT mutation 25666 FT /label="T1929M" FT /note="Thr1929Met, C>T" FT primerF 5600..5623 FT /label="3F" FT /note="primer 3F" FT amplimer 5600..5980 FT /note="amplimer 3" FT exon 5713..5921 FT /note="exon 3" FT primerR complement(5980..5957) FT /label="3R" FT /note="primer 3R" FT primerF 6171..6194 FT /label="4F" FT /note="primer 4F" FT amplimer 6171..6550 FT /note="amplimer 4" FT exon 6225..6368 FT /note="exon 4" FT primerR complement(6550..6527) FT /label="4R" FT /note="primer 4R" FT primerF 6581..6604 FT /label="5F" FT /note="primer 5F" FT amplimer 6581..6978 FT /note="amplimer 5" FT exon 6657..6813 FT /note="exon 5" FT primerR complement(6978..6955) FT /label="5R" FT /note="primer 5R" FT primerF 6677..6700 FT /label="6F" FT /note="primer 6F" FT amplimer 6677..7070 FT /note="amplimer 6" FT exon 6945..6972 FT /note="exon 6" FT primerR complement(7070..7048) FT /label="6R" FT /note="primer 6R" FT primerF 7527..7550 FT /label="7F" FT /note="primer 7F" FT amplimer 7527..7724 FT /note="amplimer 7" FT exon 7581..7689 FT /note="exon 7" FT primerR complement(7724..7701) FT /label="7R" FT /note="primer 7R" FT primerF 7701..7724 FT /label="8F" FT /note="primer 8F" FT amplimer 7701..7900 FT /note="amplimer 8" FT exon 7772..7864 FT /note="exon 8" FT primerR complement(7900..7877) FT /label="8R" FT /note="primer 8R" FT primerF 7847..7867 FT /label="9F" FT /note="primer 9F" FT amplimer 7847..8127 FT /note="amplimer 9" FT exon 7968..8031 FT /note="exon 9" FT primerR complement(8127..8106) FT /label="9R" FT /note="primer 9R" FT primerF 8362..8385 FT /label="10F" FT /note="primer 10F" FT amplimer 8362..8613 FT /note="amplimer 10" FT exon 8450..8548 FT /note="exon 10" FT primerR complement(8613..8593) FT /label="10R" FT /note="primer 10R" FT primerF 8701..8724 FT /label="11F" FT /note="primer 11F" FT amplimer 8701..8984 FT /note="amplimer 11" FT exon 8788..8891 FT /note="exon 11" FT primerR complement(8984..8961) FT /label="11R" FT /note="primer 11R" FT primerF 9435..9458 FT /label="12F" FT /note="primer 12F" FT amplimer 9435..9707 FT /note="amplimer 12" FT exon 9538..9676 FT /note="exon 12" FT primerR complement(9707..9688) FT /label="12R" FT /note="primer 12R" FT primerF 10052..10076 FT /label="13F" FT /note="primer 13F" FT amplimer 10052..10237 FT /note="amplimer 13" FT exon 10095..10213 FT /note="exon 13" FT primerR complement(10237..10213) FT /label="13R" FT /note="primer 13R" FT primerF 10282..10306 FT /label="14F" FT /note="primer 14F" FT amplimer 10282..10539 FT /note="amplimer 14" FT exon 10338..10487 FT /note="exon 14" FT primerR complement(10539..10515) FT /label="14R" FT /note="primer 14R" FT primerF 10725..10749 FT /label="15F" FT /note="primer 15F" FT amplimer 10725..10971 FT /note="amplimer 15" FT exon 10772..10942 FT /note="exon 15" FT primerR complement(10971..10947) FT /label="15R" FT /note="primer 15R" FT primerF 11410..11434 FT /label="16F" FT /note="primer 16F" FT amplimer 11410..11987 FT /note="amplimer 16" FT exon 11547..11856 FT /note="exon 16" FT primerR complement(11987..11963) FT /label="16R" FT /note="primer 16R" FT primerF 12033..12056 FT /label="17F" FT /note="primer 17F" FT amplimer 12033..12391 FT /note="amplimer 17" FT exon 12128..12195 FT /note="exon 17" FT primerR complement(12391..12370) FT /label="17R" FT /note="primer 17R" FT primerF 12451..12474 FT /label="18F" FT /note="primer 18F" FT amplimer 12451..12750 FT /note="amplimer 18" FT exon 12570..12657 FT /note="exon 18" FT primerR complement(12750..12727) FT /label="18R" FT /note="primer 18R" FT primerF 13278..13301 FT /label="19F" FT /note="primer 19F" FT amplimer 13278..13600 FT /note="amplimer 19" FT exon 13352..13469 FT /note="exon 19" FT primerR complement(13600..13577) FT /label="19R" FT /note="primer 19R" FT primerF 13471..13494 FT /label="20F" FT /note="primer 20F" FT amplimer 13471..13800 FT /note="amplimer 20" FT exon 13615..13738 FT /note="exon 20" FT primerR complement(13800..13777) FT /label="20R" FT /note="primer 20R" FT primerF 13927..13950 FT /label="21F" FT /note="primer 21F" FT amplimer 13927..14300 FT /note="amplimer 21" FT exon 14015..14151 FT /note="exon 21" FT primerR complement(14300..14277) FT /label="21R" FT /note="primer 21R" FT primerF 14351..14374 FT /label="22F" FT /note="primer 22F" FT amplimer 14351..14740 FT /note="amplimer 22" FT exon 14408..14663 FT /note="exon 22" FT primerR complement(14740..14717) FT /label="22R" FT /note="primer 22R" FT primerF 15191..15214 FT /label="23F" FT /note="primer 23F" FT amplimer 15191..15580 FT /note="amplimer 23" FT exon 15283..15525 FT /note="exon 23" FT primerR complement(15580..15557) FT /label="23R" FT /note="primer 23R" FT primerF 15651..15674 FT /label="24F" FT /note="primer 24F" FT amplimer 15651..15940 FT /note="amplimer 24" FT exon 15709..15885 FT /note="exon 24" FT primerR complement(15940..15917) FT /label="24R" FT /note="primer 24R" FT primerF 16944..16967 FT /label="25F" FT /note="primer 25F" FT amplimer 16944..17451 FT /note="amplimer 25" FT exon 17101..17246 FT /note="exon 25" FT primerR complement(17451..17428) FT /label="25R" FT /note="primer 25R" FT primerF 18282..18305 FT /label="26F" FT /note="primer 26F" FT amplimer 18282..18587 FT /note="amplimer 26" FT exon 18377..18467 FT /note="exon 26" FT primerR complement(18587..18564) FT /label="26R" FT /note="primer 26R" FT exon 19193..19582 FT /note="exon 27" FT exon 19818..19944 FT /note="exon 28" FT exon 20132..20250 FT /note="exon 29" FT exon 21021..21217 FT /note="exon 30" FT exon 21741..21924 FT /note="exon 31" FT exon 22109..22274 FT /note="exon 32" FT exon 22435..22559 FT /note="exon 33" FT exon 23115..23423 FT /note="exon 34" FT exon 23595..23798 FT /note="exon 35" FT exon 23921..24046 FT /note="exon 36" FT exon 24157..24432 FT /note="exon 37" FT exon 25327..25422 FT /note="exon 38" FT exon 25536..25670 FT /note="exon 39" FT exon 26558..26689 FT /note="exon 40"