ENST00000375254.8:c.15265G>T
MANE Select
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ENSP00000364403.3:p.Ala5089Ser
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ENST00000375224.1:c.2386G>T
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ENSP00000364372.1:p.Ala796Ser
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ENST00000375225.7:c.490G>T
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ENSP00000364373.3:p.Ala164Ser
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ENST00000375254.7:c.15265G>T
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ENSP00000364403.3:p.Ala5089Ser
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ENST00000459947.5:n.3272G>T
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NM_020765.2:c.15265G>T
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NP_065816.2:p.Ala5089Ser
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XM_011541108.1:c.15418G>T
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XP_011539410.1:p.Ala5140Ser
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XM_011541109.1:c.15415G>T
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XP_011539411.1:p.Ala5139Ser
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XM_011541110.1:c.15415G>T
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XP_011539412.1:p.Ala5139Ser
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XM_011541111.1:c.15415G>T
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XP_011539413.1:p.Ala5139Ser
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XM_011541112.1:c.15403G>T
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XP_011539414.1:p.Ala5135Ser
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XM_011541113.1:c.15400G>T
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XP_011539415.1:p.Ala5134Ser
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XM_011541114.1:c.15400G>T
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XP_011539416.1:p.Ala5134Ser
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XM_011541115.1:c.15394G>T
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XP_011539417.1:p.Ala5132Ser
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XM_011541116.1:c.15385G>T
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XP_011539418.1:p.Ala5129Ser
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XM_011541117.1:c.15334G>T
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XP_011539419.1:p.Ala5112Ser
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XM_011541118.1:c.15331G>T
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XP_011539420.1:p.Ala5111Ser
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XM_011541119.1:c.15298G>T
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XP_011539421.1:p.Ala5100Ser
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XM_011541120.1:c.15295G>T
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XP_011539422.1:p.Ala5099Ser
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XM_011541121.1:c.15262G>T
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XP_011539423.1:p.Ala5088Ser
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XM_011541108.3:c.15532G>T
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XP_011539410.2:p.Ala5178Ser
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XM_011541109.3:c.15529G>T
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XP_011539411.2:p.Ala5177Ser
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XM_011541110.3:c.15529G>T
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XP_011539412.2:p.Ala5177Ser
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XM_011541111.3:c.15529G>T
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XP_011539413.2:p.Ala5177Ser
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XM_011541112.3:c.15517G>T
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XP_011539414.2:p.Ala5173Ser
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XM_011541113.3:c.15514G>T
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XP_011539415.2:p.Ala5172Ser
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XM_011541114.3:c.15514G>T
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XP_011539416.2:p.Ala5172Ser
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XM_011541115.3:c.15508G>T
|
XP_011539417.2:p.Ala5170Ser
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XM_011541116.3:c.15499G>T
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XP_011539418.2:p.Ala5167Ser
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XM_011541117.3:c.15448G>T
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XP_011539419.2:p.Ala5150Ser
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XM_011541118.3:c.15445G>T
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XP_011539420.2:p.Ala5149Ser
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XM_011541119.3:c.15412G>T
|
XP_011539421.2:p.Ala5138Ser
|
|
XM_011541120.3:c.15409G>T
|
XP_011539422.2:p.Ala5137Ser
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|
XM_011541121.3:c.15376G>T
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XP_011539423.2:p.Ala5126Ser
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XM_017000822.2:c.15511G>T
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XP_016856311.2:p.Ala5171Ser
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XM_017000823.2:c.15484G>T
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XP_016856312.2:p.Ala5162Ser
|
|
XM_017000824.2:c.15430G>T
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XP_016856313.2:p.Ala5144Ser
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XM_017000825.2:c.15415G>T
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XP_016856314.2:p.Ala5139Ser
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|
XM_017000826.2:c.15412G>T
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XP_016856315.2:p.Ala5138Ser
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|
XM_017000827.2:c.15397G>T
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XP_016856316.2:p.Ala5133Ser
|
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XM_017000828.2:c.15373G>T
|
XP_016856317.2:p.Ala5125Ser
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XM_017000829.2:c.15325G>T
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XP_016856318.2:p.Ala5109Ser
|
|
XM_017000830.2:c.15274G>T
|
XP_016856319.2:p.Ala5092Ser
|
|
NM_020765.3:c.15265G>T
MANE Select
|
NP_065816.2:p.Ala5089Ser
|
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