ENST00000585465.3:c.*2832C>A
|
ENSP00000490268.2:n.*2832C>A
|
|
ENST00000585748.3:c.859C>A
|
ENSP00000477641.2:p.Pro287Thr
|
|
ENST00000585851.2:c.1057C>A
|
ENSP00000467912.2:p.Pro353Thr
|
|
ENST00000326873.12:c.1231C>A
MANE Select
|
ENSP00000324856.6:p.Pro411Thr
|
|
ENST00000326873.11:c.1231C>A
|
ENSP00000324856.6:p.Pro411Thr
|
|
ENST00000585465.2:n.2964C>A
|
|
|
ENST00000586243.5:c.1230C>A
|
ENSP00000467240.2:p.Pro410=
|
|
ENST00000589152.5:n.1929C>A
|
|
|
NM_000455.4:c.1231C>A , LRG_319t1:c.1231C>A
|
NP_000446.1:p.Pro411Thr
|
|
XM_005259617.1:c.1226C>A
|
XP_005259674.1:p.Pro409His
|
|
XM_011528209.1:c.1004C>A
|
XP_011526511.1:p.Pro335His
|
|
XM_005259617.3:c.1226C>A
|
XP_005259674.1:p.Pro409His
|
|
XM_011528209.2:c.1004C>A
|
XP_011526511.1:p.Pro335His
|
|
XR_001753738.2:n.2037C>A
|
|
|
XR_001753740.2:n.2007C>A
|
|
|
NM_000455.5:c.1231C>A
MANE Select
|
NP_000446.1:p.Pro411Thr
|
|