ENST00000614293.5:c.2127T>G
|
ENSP00000481105.2:p.Asp709Glu
|
|
ENST00000341511.11:c.2037T>G
MANE Select
|
ENSP00000344155.6:p.Asp679Glu
|
|
ENST00000265662.9:c.2037T>G
|
ENSP00000265662.5:p.Asp679Glu
|
|
ENST00000341511.10:c.2037T>G
|
ENSP00000344155.6:p.Asp679Glu
|
|
ENST00000371605.7:c.2034T>G
|
ENSP00000360666.3:p.Asp678Glu
|
|
ENST00000459850.5:n.2167T>G
|
|
|
ENST00000466707.1:n.85T>G
|
|
|
ENST00000479446.5:c.86T>G
|
|
|
ENST00000487109.5:c.2124T>G
|
ENSP00000418662.1:p.Asp708Glu
|
|
ENST00000488535.2:c.78T>G
|
ENSP00000419850.1:p.Asp26Glu
|
|
ENST00000614293.4:c.2127T>G
|
ENSP00000481105.1:p.Asp709Glu
|
|
NM_001606.4:c.2037T>G
|
NP_001597.2:p.Asp679Glu
|
|
NM_212533.2:c.2127T>G
|
NP_997698.1:p.Asp709Glu
|
|
XM_006716996.2:c.2034T>G
|
XP_006717059.1:p.Asp678Glu
|
|
XM_011518346.1:c.2124T>G
|
XP_011516648.1:p.Asp708Glu
|
|
XM_006716996.4:c.2034T>G
|
XP_006717059.1:p.Asp678Glu
|
|
XR_001746224.1:n.2161T>G
|
|
|
NM_001606.5:c.2037T>G
MANE Select
|
NP_001597.2:p.Asp679Glu
|
|
NM_212533.3:c.2127T>G
|
NP_997698.1:p.Asp709Glu
|
|