ENST00000585465.3:c.*2773G>T
|
ENSP00000490268.2:n.*2773G>T
|
|
ENST00000585748.3:c.800G>T
|
ENSP00000477641.2:p.Cys267Phe
|
|
ENST00000585851.2:c.998G>T
|
ENSP00000467912.2:p.Cys333Phe
|
|
ENST00000326873.12:c.1172G>T
MANE Select
|
ENSP00000324856.6:p.Cys391Phe
|
|
ENST00000326873.11:c.1172G>T
|
ENSP00000324856.6:p.Cys391Phe
|
|
ENST00000585465.2:n.2905G>T
|
|
|
ENST00000586243.5:c.1172G>T
|
ENSP00000467240.2:p.Cys391Phe
|
|
ENST00000589152.5:n.1870G>T
|
|
|
NM_000455.4:c.1172G>T , LRG_319t1:c.1172G>T
|
NP_000446.1:p.Cys391Phe
|
|
XM_005259617.1:c.1167G>T
|
XP_005259674.1:p.Val389=
|
|
XM_011528209.1:c.945G>T
|
XP_011526511.1:p.Val315=
|
|
XM_005259617.3:c.1167G>T
|
XP_005259674.1:p.Val389=
|
|
XM_011528209.2:c.945G>T
|
XP_011526511.1:p.Val315=
|
|
XR_001753738.2:n.1978G>T
|
|
|
XR_001753740.2:n.1948G>T
|
|
|
NM_000455.5:c.1172G>T
MANE Select
|
NP_000446.1:p.Cys391Phe
|
|