ENST00000585465.3:c.*2785C>G
|
ENSP00000490268.2:n.*2785C>G
|
|
ENST00000585748.3:c.812C>G
|
ENSP00000477641.2:p.Thr271Arg
|
|
ENST00000585851.2:c.1010C>G
|
ENSP00000467912.2:p.Thr337Arg
|
|
ENST00000326873.12:c.1184C>G
MANE Select
|
ENSP00000324856.6:p.Thr395Arg
|
|
ENST00000326873.11:c.1184C>G
|
ENSP00000324856.6:p.Thr395Arg
|
|
ENST00000585465.2:n.2917C>G
|
|
|
ENST00000586243.5:c.1184C>G
|
ENSP00000467240.2:p.Thr395Arg
|
|
ENST00000589152.5:n.1882C>G
|
|
|
NM_000455.4:c.1184C>G , LRG_319t1:c.1184C>G
|
NP_000446.1:p.Thr395Arg
|
|
XM_005259617.1:c.1179C>G
|
XP_005259674.1:p.His393Gln
|
|
XM_011528209.1:c.957C>G
|
XP_011526511.1:p.His319Gln
|
|
XM_005259617.3:c.1179C>G
|
XP_005259674.1:p.His393Gln
|
|
XM_011528209.2:c.957C>G
|
XP_011526511.1:p.His319Gln
|
|
XR_001753738.2:n.1990C>G
|
|
|
XR_001753740.2:n.1960C>G
|
|
|
NM_000455.5:c.1184C>G
MANE Select
|
NP_000446.1:p.Thr395Arg
|
|