ENST00000585465.3:c.*2784A>G
|
ENSP00000490268.2:n.*2784A>G
|
|
ENST00000585748.3:c.811A>G
|
ENSP00000477641.2:p.Thr271Ala
|
|
ENST00000585851.2:c.1009A>G
|
ENSP00000467912.2:p.Thr337Ala
|
|
ENST00000326873.12:c.1183A>G
MANE Select
|
ENSP00000324856.6:p.Thr395Ala
|
|
ENST00000326873.11:c.1183A>G
|
ENSP00000324856.6:p.Thr395Ala
|
|
ENST00000585465.2:n.2916A>G
|
|
|
ENST00000586243.5:c.1183A>G
|
ENSP00000467240.2:p.Thr395Ala
|
|
ENST00000589152.5:n.1881A>G
|
|
|
NM_000455.4:c.1183A>G , LRG_319t1:c.1183A>G
|
NP_000446.1:p.Thr395Ala
|
|
XM_005259617.1:c.1178A>G
|
XP_005259674.1:p.His393Arg
|
|
XM_011528209.1:c.956A>G
|
XP_011526511.1:p.His319Arg
|
|
XM_005259617.3:c.1178A>G
|
XP_005259674.1:p.His393Arg
|
|
XM_011528209.2:c.956A>G
|
XP_011526511.1:p.His319Arg
|
|
XR_001753738.2:n.1989A>G
|
|
|
XR_001753740.2:n.1959A>G
|
|
|
NM_000455.5:c.1183A>G
MANE Select
|
NP_000446.1:p.Thr395Ala
|
|