ENST00000585465.3:c.*2820G>A
|
ENSP00000490268.2:n.*2820G>A
|
|
ENST00000585748.3:c.847G>A
|
ENSP00000477641.2:p.Glu283Lys
|
|
ENST00000585851.2:c.1045G>A
|
ENSP00000467912.2:p.Glu349Lys
|
|
ENST00000326873.12:c.1219G>A
MANE Select
|
ENSP00000324856.6:p.Glu407Lys
|
|
ENST00000326873.11:c.1219G>A
|
ENSP00000324856.6:p.Glu407Lys
|
|
ENST00000585465.2:n.2952G>A
|
|
|
ENST00000586243.5:c.1219G>A
|
ENSP00000467240.2:p.Glu407Lys
|
|
ENST00000589152.5:n.1917G>A
|
|
|
NM_000455.4:c.1219G>A , LRG_319t1:c.1219G>A
|
NP_000446.1:p.Glu407Lys
|
|
XM_005259617.1:c.1214G>A
|
XP_005259674.1:p.Gly405Glu
|
|
XM_011528209.1:c.992G>A
|
XP_011526511.1:p.Gly331Glu
|
|
XM_005259617.3:c.1214G>A
|
XP_005259674.1:p.Gly405Glu
|
|
XM_011528209.2:c.992G>A
|
XP_011526511.1:p.Gly331Glu
|
|
XR_001753738.2:n.2025G>A
|
|
|
XR_001753740.2:n.1995G>A
|
|
|
NM_000455.5:c.1219G>A
MANE Select
|
NP_000446.1:p.Glu407Lys
|
|