ENST00000379727.8:c.1306G>T
MANE Select
|
ENSP00000369050.3:p.Asp436Tyr
|
|
ENST00000379727.7:c.1306G>T
|
ENSP00000369050.3:p.Asp436Tyr
|
|
ENST00000395048.6:c.1306G>T
|
ENSP00000378488.2:p.Asp436Tyr
|
|
ENST00000395049.8:c.1219G>T
|
ENSP00000378489.4:p.Asp407Tyr
|
|
ENST00000562201.5:c.*543G>T
|
ENSP00000455340.1:n.*543G>T
|
|
ENST00000564596.5:c.*241G>T
|
ENSP00000457668.1:n.*241G>T
|
|
ENST00000566503.1:c.523G>T
|
ENSP00000455846.1:p.Asp175Tyr
|
|
ENST00000567032.5:c.1306G>T
|
ENSP00000456585.1:p.Asp436Tyr
|
|
ENST00000569630.5:c.*895G>T
|
ENSP00000455051.1:n.*895G>T
|
|
ENST00000612821.4:c.1222G>T
|
ENSP00000479744.1:p.Asp408Tyr
|
|
ENST00000617691.4:c.1219G>T
|
ENSP00000482863.1:p.Asp407Tyr
|
|
NM_000499.3:c.1306G>T
|
NP_000490.1:p.Asp436Tyr
|
|
XM_005254185.1:c.1306G>T
|
XP_005254242.1:p.Asp436Tyr
|
|
NM_000499.5:c.1306G>T
|
NP_000490.1:p.Asp436Tyr
|
|
NM_001319216.2:c.1219G>T
|
NP_001306145.1:p.Asp407Tyr
|
|
NM_001319217.2:c.1306G>T
MANE Select
|
NP_001306146.1:p.Asp436Tyr
|
|