ENST00000585465.3:c.*2825C>A
|
ENSP00000490268.2:n.*2825C>A
|
|
ENST00000585748.3:c.852C>A
|
ENSP00000477641.2:p.Gly284=
|
|
ENST00000585851.2:c.1050C>A
|
ENSP00000467912.2:p.Gly350=
|
|
ENST00000326873.12:c.1224C>A
MANE Select
|
ENSP00000324856.6:p.Gly408=
|
|
ENST00000326873.11:c.1224C>A
|
ENSP00000324856.6:p.Gly408=
|
|
ENST00000585465.2:n.2957C>A
|
|
|
ENST00000586243.5:c.1223C>A
|
ENSP00000467240.2:p.Ala408Asp
|
|
ENST00000589152.5:n.1922C>A
|
|
|
NM_000455.4:c.1224C>A , LRG_319t1:c.1224C>A
|
NP_000446.1:p.Gly408=
|
|
XM_005259617.1:c.1219C>A
|
XP_005259674.1:p.Pro407Thr
|
|
XM_011528209.1:c.997C>A
|
XP_011526511.1:p.Pro333Thr
|
|
XM_005259617.3:c.1219C>A
|
XP_005259674.1:p.Pro407Thr
|
|
XM_011528209.2:c.997C>A
|
XP_011526511.1:p.Pro333Thr
|
|
XR_001753738.2:n.2030C>A
|
|
|
XR_001753740.2:n.2000C>A
|
|
|
NM_000455.5:c.1224C>A
MANE Select
|
NP_000446.1:p.Gly408=
|
|