ENST00000264414.9:c.1262T>C
MANE Select
|
ENSP00000264414.4:p.Phe421Ser
|
|
ENST00000264414.8:c.1262T>C
|
ENSP00000264414.4:p.Phe421Ser
|
|
ENST00000344951.8:c.1064T>C
|
ENSP00000343601.4:p.Phe355Ser
|
|
ENST00000409096.5:c.1190T>C
|
ENSP00000387200.1:p.Phe397Ser
|
|
ENST00000409777.5:c.1190T>C
|
ENSP00000386525.1:p.Phe397Ser
|
|
ENST00000481135.1:n.558T>C
|
|
|
ENST00000617432.4:c.-15T>C
|
ENSP00000477851.1:n.-15T>C
|
|
NM_001257197.1:c.1064T>C
|
NP_001244126.1:p.Phe355Ser
|
|
NM_001257198.1:c.1280T>C
|
NP_001244127.1:p.Phe427Ser
|
|
NM_003590.4:c.1262T>C
|
NP_003581.1:p.Phe421Ser
|
|
XM_006712800.2:c.1229T>C
|
XP_006712863.2:p.Phe410Ser
|
|
XM_011511994.1:c.1115T>C
|
XP_011510296.1:p.Phe372Ser
|
|
XM_011511995.1:c.1220T>C
|
XP_011510297.1:p.Phe407Ser
|
|
XM_011511996.1:c.1070T>C
|
XP_011510298.1:p.Phe357Ser
|
|
XM_011511997.1:c.962T>C
|
XP_011510299.1:p.Phe321Ser
|
|
XM_011511994.3:c.1115T>C
|
XP_011510296.1:p.Phe372Ser
|
|
XM_011511996.2:c.1070T>C
|
XP_011510298.1:p.Phe357Ser
|
|
NM_003590.5:c.1262T>C
MANE Select
|
NP_003581.1:p.Phe421Ser
|
|
NM_001257198.2:c.1280T>C
|
NP_001244127.1:p.Phe427Ser
|
|
NM_001257197.2:c.1064T>C
|
NP_001244126.1:p.Phe355Ser
|
|