ENST00000585465.3:c.*2874C>G
|
ENSP00000490268.2:n.*2874C>G
|
|
ENST00000585748.3:c.901C>G
|
ENSP00000477641.2:p.Arg301Gly
|
|
ENST00000585851.2:c.1099C>G
|
ENSP00000467912.2:p.Arg367Gly
|
|
ENST00000326873.12:c.1273C>G
MANE Select
|
ENSP00000324856.6:p.Arg425Gly
|
|
ENST00000326873.11:c.1273C>G
|
ENSP00000324856.6:p.Arg425Gly
|
|
ENST00000585465.2:n.3006C>G
|
|
|
ENST00000586243.5:c.1270C>G
|
ENSP00000467240.2:p.Arg424Gly
|
|
ENST00000589152.5:n.1971C>G
|
|
|
NM_000455.4:c.1273C>G , LRG_319t1:c.1273C>G
|
NP_000446.1:p.Arg425Gly
|
|
XM_005259617.1:c.1268C>G
|
XP_005259674.1:p.Pro423Arg
|
|
XM_011528209.1:c.1046C>G
|
XP_011526511.1:p.Pro349Arg
|
|
XM_005259617.3:c.1268C>G
|
XP_005259674.1:p.Pro423Arg
|
|
XM_011528209.2:c.1046C>G
|
XP_011526511.1:p.Pro349Arg
|
|
XR_001753738.2:n.2079C>G
|
|
|
XR_001753740.2:n.2049C>G
|
|
|
NM_000455.5:c.1273C>G
MANE Select
|
NP_000446.1:p.Arg425Gly
|
|