ENST00000264414.9:c.1261T>G
MANE Select
|
ENSP00000264414.4:p.Phe421Val
|
|
ENST00000264414.8:c.1261T>G
|
ENSP00000264414.4:p.Phe421Val
|
|
ENST00000344951.8:c.1063T>G
|
ENSP00000343601.4:p.Phe355Val
|
|
ENST00000409096.5:c.1189T>G
|
ENSP00000387200.1:p.Phe397Val
|
|
ENST00000409777.5:c.1189T>G
|
ENSP00000386525.1:p.Phe397Val
|
|
ENST00000481135.1:n.557T>G
|
|
|
ENST00000617432.4:c.-16T>G
|
ENSP00000477851.1:n.-16T>G
|
|
NM_001257197.1:c.1063T>G
|
NP_001244126.1:p.Phe355Val
|
|
NM_001257198.1:c.1279T>G
|
NP_001244127.1:p.Phe427Val
|
|
NM_003590.4:c.1261T>G
|
NP_003581.1:p.Phe421Val
|
|
XM_006712800.2:c.1228T>G
|
XP_006712863.2:p.Phe410Val
|
|
XM_011511994.1:c.1114T>G
|
XP_011510296.1:p.Phe372Val
|
|
XM_011511995.1:c.1219T>G
|
XP_011510297.1:p.Phe407Val
|
|
XM_011511996.1:c.1069T>G
|
XP_011510298.1:p.Phe357Val
|
|
XM_011511997.1:c.961T>G
|
XP_011510299.1:p.Phe321Val
|
|
XM_011511994.3:c.1114T>G
|
XP_011510296.1:p.Phe372Val
|
|
XM_011511996.2:c.1069T>G
|
XP_011510298.1:p.Phe357Val
|
|
NM_003590.5:c.1261T>G
MANE Select
|
NP_003581.1:p.Phe421Val
|
|
NM_001257198.2:c.1279T>G
|
NP_001244127.1:p.Phe427Val
|
|
NM_001257197.2:c.1063T>G
|
NP_001244126.1:p.Phe355Val
|
|