ENST00000585465.3:c.851A>T
|
ENSP00000490268.2:p.Asp284Val
|
|
ENST00000585748.3:c.479A>T
|
ENSP00000477641.2:p.Asp160Val
|
|
ENST00000585851.2:c.677A>T
|
ENSP00000467912.2:p.Asp226Val
|
|
ENST00000326873.12:c.851A>T
MANE Select
|
ENSP00000324856.6:p.Asp284Val
|
|
ENST00000652231.1:c.851A>T
|
ENSP00000498804.1:p.Asp284Val
|
|
ENST00000326873.11:c.851A>T
|
ENSP00000324856.6:p.Asp284Val
|
|
ENST00000586243.5:c.851A>T
|
ENSP00000467240.2:p.Asp284Val
|
|
ENST00000586358.5:n.749A>T
|
|
|
ENST00000589152.5:n.941A>T
|
|
|
ENST00000591133.2:n.822A>T
|
|
|
NM_000455.4:c.851A>T , LRG_319t1:c.851A>T
|
NP_000446.1:p.Asp284Val
|
|
XM_005259617.1:c.851A>T
|
XP_005259674.1:p.Asp284Val
|
|
XM_005259618.3:c.851A>T
|
XP_005259675.1:p.Asp284Val
|
|
XM_011528209.1:c.629A>T
|
XP_011526511.1:p.Asp210Val
|
|
XR_936204.1:n.1476A>T
|
|
|
XM_005259617.3:c.851A>T
|
XP_005259674.1:p.Asp284Val
|
|
XM_011528209.2:c.629A>T
|
XP_011526511.1:p.Asp210Val
|
|
XR_001753738.2:n.1476A>T
|
|
|
XR_001753739.1:n.1476A>T
|
|
|
XR_001753740.2:n.1476A>T
|
|
|
NM_000455.5:c.851A>T
MANE Select
|
NP_000446.1:p.Asp284Val
|
|