ENST00000585465.3:c.*2889T>A
|
ENSP00000490268.2:n.*2889T>A
|
|
ENST00000585748.3:c.916T>A
|
ENSP00000477641.2:p.Cys306Ser
|
|
ENST00000585851.2:c.1114T>A
|
ENSP00000467912.2:p.Cys372Ser
|
|
ENST00000326873.12:c.1288T>A
MANE Select
|
ENSP00000324856.6:p.Cys430Ser
|
|
ENST00000326873.11:c.1288T>A
|
ENSP00000324856.6:p.Cys430Ser
|
|
ENST00000585465.2:n.3021T>A
|
|
|
ENST00000586243.5:c.1285T>A
|
ENSP00000467240.2:p.Cys429Ser
|
|
ENST00000589152.5:n.1986T>A
|
|
|
NM_000455.4:c.1288T>A , LRG_319t1:c.1288T>A
|
NP_000446.1:p.Cys430Ser
|
|
XM_005259617.1:c.1283T>A
|
XP_005259674.1:p.Leu428Gln
|
|
XM_011528209.1:c.1061T>A
|
XP_011526511.1:p.Leu354Gln
|
|
XM_005259617.3:c.1283T>A
|
XP_005259674.1:p.Leu428Gln
|
|
XM_011528209.2:c.1061T>A
|
XP_011526511.1:p.Leu354Gln
|
|
XR_001753738.2:n.2094T>A
|
|
|
XR_001753740.2:n.2064T>A
|
|
|
NM_000455.5:c.1288T>A
MANE Select
|
NP_000446.1:p.Cys430Ser
|
|