ENST00000585465.3:c.*2729G>T
|
ENSP00000490268.2:n.*2729G>T
|
|
ENST00000585748.3:c.756G>T
|
ENSP00000477641.2:p.Glu252Asp
|
|
ENST00000585851.2:c.954G>T
|
ENSP00000467912.2:p.Glu318Asp
|
|
ENST00000326873.12:c.1128G>T
MANE Select
|
ENSP00000324856.6:p.Glu376Asp
|
|
ENST00000326873.11:c.1128G>T
|
ENSP00000324856.6:p.Glu376Asp
|
|
ENST00000585465.2:n.2861G>T
|
|
|
ENST00000586243.5:c.1128G>T
|
ENSP00000467240.2:p.Glu376Asp
|
|
ENST00000589152.5:n.1826G>T
|
|
|
NM_000455.4:c.1128G>T , LRG_319t1:c.1128G>T
|
NP_000446.1:p.Glu376Asp
|
|
XM_005259617.1:c.1123G>T
|
XP_005259674.1:p.Gly375Cys
|
|
XM_011528209.1:c.901G>T
|
XP_011526511.1:p.Gly301Cys
|
|
XM_005259617.3:c.1123G>T
|
XP_005259674.1:p.Gly375Cys
|
|
XM_011528209.2:c.901G>T
|
XP_011526511.1:p.Gly301Cys
|
|
XR_001753738.2:n.1934G>T
|
|
|
XR_001753740.2:n.1904G>T
|
|
|
NM_000455.5:c.1128G>T
MANE Select
|
NP_000446.1:p.Glu376Asp
|
|