ENST00000585465.3:c.*2716T>A
|
ENSP00000490268.2:n.*2716T>A
|
|
ENST00000585748.3:c.743T>A
|
ENSP00000477641.2:p.Val248Asp
|
|
ENST00000585851.2:c.941T>A
|
ENSP00000467912.2:p.Val314Asp
|
|
ENST00000326873.12:c.1115T>A
MANE Select
|
ENSP00000324856.6:p.Val372Asp
|
|
ENST00000326873.11:c.1115T>A
|
ENSP00000324856.6:p.Val372Asp
|
|
ENST00000585465.2:n.2848T>A
|
|
|
ENST00000586243.5:c.1115T>A
|
ENSP00000467240.2:p.Val372Asp
|
|
ENST00000589152.5:n.1813T>A
|
|
|
NM_000455.4:c.1115T>A , LRG_319t1:c.1115T>A
|
NP_000446.1:p.Val372Asp
|
|
XM_005259617.1:c.1110T>A
|
XP_005259674.1:p.Gly370=
|
|
XM_011528209.1:c.888T>A
|
XP_011526511.1:p.Gly296=
|
|
XM_005259617.3:c.1110T>A
|
XP_005259674.1:p.Gly370=
|
|
XM_011528209.2:c.888T>A
|
XP_011526511.1:p.Gly296=
|
|
XR_001753738.2:n.1921T>A
|
|
|
XR_001753740.2:n.1891T>A
|
|
|
NM_000455.5:c.1115T>A
MANE Select
|
NP_000446.1:p.Val372Asp
|
|