ENST00000456935.7:c.1146T>G
MANE Select
|
ENSP00000395473.2:p.Asp382Glu
|
|
ENST00000221363.8:c.1143T>G
|
ENSP00000221363.4:p.Asp381Glu
|
|
ENST00000456935.6:c.1146T>G
|
ENSP00000395473.2:p.Asp382Glu
|
|
ENST00000465830.1:n.310T>G
|
|
|
ENST00000466794.5:n.1045T>G
|
|
|
ENST00000495617.1:n.280+423T>G
|
|
|
NM_000528.3:c.1146T>G
|
NP_000519.2:p.Asp382Glu
|
|
NM_001173498.1:c.1143T>G
|
NP_001166969.1:p.Asp381Glu
|
|
XM_005259913.1:c.1149T>G
|
XP_005259970.1:p.Asp383Glu
|
|
XM_011528017.1:c.45T>G
|
XP_011526319.1:p.Asp15Glu
|
|
XM_005259913.2:c.1149T>G
|
XP_005259970.1:p.Asp383Glu
|
|
XM_024451518.1:c.45T>G
|
XP_024307286.1:p.Asp15Glu
|
|
NM_000528.4:c.1146T>G
MANE Select
|
NP_000519.2:p.Asp382Glu
|
|
NM_001173498.2:c.1143T>G
|
NP_001166969.1:p.Asp381Glu
|
|