ENST00000585465.3:c.*2889T>G
|
ENSP00000490268.2:n.*2889T>G
|
|
ENST00000585748.3:c.916T>G
|
ENSP00000477641.2:p.Cys306Gly
|
|
ENST00000585851.2:c.1114T>G
|
ENSP00000467912.2:p.Cys372Gly
|
|
ENST00000326873.12:c.1288T>G
MANE Select
|
ENSP00000324856.6:p.Cys430Gly
|
|
ENST00000326873.11:c.1288T>G
|
ENSP00000324856.6:p.Cys430Gly
|
|
ENST00000585465.2:n.3021T>G
|
|
|
ENST00000586243.5:c.1285T>G
|
ENSP00000467240.2:p.Cys429Gly
|
|
ENST00000589152.5:n.1986T>G
|
|
|
NM_000455.4:c.1288T>G , LRG_319t1:c.1288T>G
|
NP_000446.1:p.Cys430Gly
|
|
XM_005259617.1:c.1283T>G
|
XP_005259674.1:p.Leu428Arg
|
|
XM_011528209.1:c.1061T>G
|
XP_011526511.1:p.Leu354Arg
|
|
XM_005259617.3:c.1283T>G
|
XP_005259674.1:p.Leu428Arg
|
|
XM_011528209.2:c.1061T>G
|
XP_011526511.1:p.Leu354Arg
|
|
XR_001753738.2:n.2094T>G
|
|
|
XR_001753740.2:n.2064T>G
|
|
|
NM_000455.5:c.1288T>G
MANE Select
|
NP_000446.1:p.Cys430Gly
|
|