ENST00000585465.3:c.*2918A>G
|
ENSP00000490268.2:n.*2918A>G
|
|
ENST00000585748.3:c.*15A>G
|
ENSP00000477641.2:n.*15A>G
|
|
ENST00000585851.2:c.*15A>G
|
ENSP00000467912.2:n.*15A>G
|
|
ENST00000326873.12:c.*15A>G
MANE Select
|
ENSP00000324856.6:n.*15A>G
|
|
ENST00000326873.11:c.*15A>G
|
ENSP00000324856.6:n.*15A>G
|
|
ENST00000585465.2:n.3050A>G
|
|
|
ENST00000586243.5:c.*15A>G
|
ENSP00000467240.2:n.*15A>G
|
|
ENST00000589152.5:n.2015A>G
|
|
|
NM_000455.4:c.*15A>G , LRG_319t1:c.*15A>G
|
NP_000446.1:n.*15A>G
|
|
XM_005259617.1:c.1312A>G
|
XP_005259674.1:p.Ser438Gly
|
|
XM_011528209.1:c.1090A>G
|
XP_011526511.1:p.Ser364Gly
|
|
XM_005259617.3:c.1312A>G
|
XP_005259674.1:p.Ser438Gly
|
|
XM_011528209.2:c.1090A>G
|
XP_011526511.1:p.Ser364Gly
|
|
XR_001753738.2:n.2123A>G
|
|
|
XR_001753740.2:n.2093A>G
|
|
|
NM_000455.5:c.*15A>G
MANE Select
|
NP_000446.1:n.*15A>G
|
|