ENST00000585465.3:c.850G>T
|
ENSP00000490268.2:p.Asp284Tyr
|
|
ENST00000585748.3:c.478G>T
|
ENSP00000477641.2:p.Asp160Tyr
|
|
ENST00000585851.2:c.676G>T
|
ENSP00000467912.2:p.Asp226Tyr
|
|
ENST00000326873.12:c.850G>T
MANE Select
|
ENSP00000324856.6:p.Asp284Tyr
|
|
ENST00000652231.1:c.850G>T
|
ENSP00000498804.1:p.Asp284Tyr
|
|
ENST00000326873.11:c.850G>T
|
ENSP00000324856.6:p.Asp284Tyr
|
|
ENST00000586243.5:c.850G>T
|
ENSP00000467240.2:p.Asp284Tyr
|
|
ENST00000586358.5:n.748G>T
|
|
|
ENST00000589152.5:n.940G>T
|
|
|
ENST00000591133.2:n.821G>T
|
|
|
NM_000455.4:c.850G>T , LRG_319t1:c.850G>T
|
NP_000446.1:p.Asp284Tyr
|
|
XM_005259617.1:c.850G>T
|
XP_005259674.1:p.Asp284Tyr
|
|
XM_005259618.3:c.850G>T
|
XP_005259675.1:p.Asp284Tyr
|
|
XM_011528209.1:c.628G>T
|
XP_011526511.1:p.Asp210Tyr
|
|
XR_936204.1:n.1475G>T
|
|
|
XM_005259617.3:c.850G>T
|
XP_005259674.1:p.Asp284Tyr
|
|
XM_011528209.2:c.628G>T
|
XP_011526511.1:p.Asp210Tyr
|
|
XR_001753738.2:n.1475G>T
|
|
|
XR_001753739.1:n.1475G>T
|
|
|
XR_001753740.2:n.1475G>T
|
|
|
NM_000455.5:c.850G>T
MANE Select
|
NP_000446.1:p.Asp284Tyr
|
|