ENST00000264380.9:c.3416C>A
MANE Select
|
ENSP00000264380.4:p.Ala1139Asp
|
|
ENST00000264380.8:c.3416C>A
|
ENSP00000264380.4:p.Ala1139Asp
|
|
ENST00000452564.1:c.3248C>A
|
ENSP00000405736.1:p.Ala1083Asp
|
|
NM_015040.3:c.3416C>A
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NP_055855.2:p.Ala1139Asp
|
|
XM_011510778.1:c.3452C>A
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XP_011509080.1:p.Ala1151Asp
|
|
XM_011510779.1:c.3452C>A
|
XP_011509081.1:p.Ala1151Asp
|
|
XM_011510780.1:c.3449C>A
|
XP_011509082.1:p.Ala1150Asp
|
|
XM_011510781.1:c.3434C>A
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XP_011509083.1:p.Ala1145Asp
|
|
XM_011510782.1:c.3452C>A
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XP_011509084.1:p.Ala1151Asp
|
|
XM_011510783.1:c.3284C>A
|
XP_011509085.1:p.Ala1095Asp
|
|
XM_011510784.1:c.3281C>A
|
XP_011509086.1:p.Ala1094Asp
|
|
XM_011510785.1:c.3266C>A
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XP_011509087.1:p.Ala1089Asp
|
|
XM_011510786.1:c.3161C>A
|
XP_011509088.1:p.Ala1054Asp
|
|
XM_011510787.1:c.3158C>A
|
XP_011509089.1:p.Ala1053Asp
|
|
XM_011510788.1:c.3125C>A
|
XP_011509090.1:p.Ala1042Asp
|
|
XM_011510789.1:c.2975C>A
|
XP_011509091.1:p.Ala992Asp
|
|
XM_011510790.1:c.2459C>A
|
XP_011509092.1:p.Ala820Asp
|
|
XM_011510791.1:c.2459C>A
|
XP_011509093.1:p.Ala820Asp
|
|
XM_011510792.1:c.3452C>A
|
XP_011509094.1:p.Ala1151Asp
|
|
XR_922888.1:n.3589C>A
|
|
|
XM_011510778.3:c.3452C>A
|
XP_011509080.1:p.Ala1151Asp
|
|
XM_011510779.2:c.3452C>A
|
XP_011509081.1:p.Ala1151Asp
|
|
XM_011510780.2:c.3449C>A
|
XP_011509082.1:p.Ala1150Asp
|
|
XM_011510781.3:c.3434C>A
|
XP_011509083.1:p.Ala1145Asp
|
|
XM_011510782.3:c.3452C>A
|
XP_011509084.1:p.Ala1151Asp
|
|
XM_011510783.3:c.3284C>A
|
XP_011509085.1:p.Ala1095Asp
|
|
XM_011510784.2:c.3281C>A
|
XP_011509086.1:p.Ala1094Asp
|
|
XM_011510785.3:c.3266C>A
|
XP_011509087.1:p.Ala1089Asp
|
|
XM_011510786.3:c.3161C>A
|
XP_011509088.1:p.Ala1054Asp
|
|
XM_011510789.2:c.2975C>A
|
XP_011509091.1:p.Ala992Asp
|
|
XM_011510792.3:c.3452C>A
|
XP_011509094.1:p.Ala1151Asp
|
|
XM_017003568.1:c.3398C>A
|
XP_016859057.1:p.Ala1133Asp
|
|
XM_017003569.1:c.3230C>A
|
XP_016859058.1:p.Ala1077Asp
|
|
XM_017003570.1:c.2957C>A
|
XP_016859059.1:p.Ala986Asp
|
|
XM_017003571.1:c.2807C>A
|
XP_016859060.1:p.Ala936Asp
|
|
XM_017003572.1:c.2459C>A
|
XP_016859061.1:p.Ala820Asp
|
|
XM_017003573.1:c.2459C>A
|
XP_016859062.1:p.Ala820Asp
|
|
XM_017003574.1:c.2459C>A
|
XP_016859063.1:p.Ala820Asp
|
|
NM_015040.4:c.3416C>A
MANE Select
|
NP_055855.2:p.Ala1139Asp
|
|