ENST00000585465.3:c.*2814A>G
|
ENSP00000490268.2:n.*2814A>G
|
|
ENST00000585748.3:c.841A>G
|
ENSP00000477641.2:p.Arg281Gly
|
|
ENST00000585851.2:c.1039A>G
|
ENSP00000467912.2:p.Arg347Gly
|
|
ENST00000326873.12:c.1213A>G
MANE Select
|
ENSP00000324856.6:p.Arg405Gly
|
|
ENST00000326873.11:c.1213A>G
|
ENSP00000324856.6:p.Arg405Gly
|
|
ENST00000585465.2:n.2946A>G
|
|
|
ENST00000586243.5:c.1213A>G
|
ENSP00000467240.2:p.Arg405Gly
|
|
ENST00000589152.5:n.1911A>G
|
|
|
NM_000455.4:c.1213A>G , LRG_319t1:c.1213A>G
|
NP_000446.1:p.Arg405Gly
|
|
XM_005259617.1:c.1208A>G
|
XP_005259674.1:p.Gln403Arg
|
|
XM_011528209.1:c.986A>G
|
XP_011526511.1:p.Gln329Arg
|
|
XM_005259617.3:c.1208A>G
|
XP_005259674.1:p.Gln403Arg
|
|
XM_011528209.2:c.986A>G
|
XP_011526511.1:p.Gln329Arg
|
|
XR_001753738.2:n.2019A>G
|
|
|
XR_001753740.2:n.1989A>G
|
|
|
NM_000455.5:c.1213A>G
MANE Select
|
NP_000446.1:p.Arg405Gly
|
|