ENST00000262367.10:c.7167C>G
MANE Select
|
ENSP00000262367.5:p.Val2389=
|
|
ENST00000262367.9:c.7167C>G
|
ENSP00000262367.5:p.Val2389=
|
|
ENST00000382070.7:c.7053C>G
|
ENSP00000371502.3:p.Val2351=
|
|
NM_001079846.1:c.7053C>G
|
NP_001073315.1:p.Val2351=
|
|
NM_004380.2:c.7167C>G
|
NP_004371.2:p.Val2389=
|
|
XM_005255124.3:c.7122C>G
|
XP_005255181.1:p.Val2374=
|
|
XM_005255125.3:c.6750C>G
|
XP_005255182.1:p.Val2250=
|
|
XM_006720848.2:c.6906C>G
|
XP_006720911.1:p.Val2302=
|
|
XM_011522380.1:c.7113C>G
|
XP_011520682.1:p.Val2371=
|
|
XM_011522381.1:c.6414C>G
|
XP_011520683.1:p.Val2138=
|
|
XM_005255124.4:c.7122C>G
|
XP_005255181.1:p.Val2374=
|
|
XM_005255125.4:c.6750C>G
|
XP_005255182.1:p.Val2250=
|
|
XM_006720848.3:c.6906C>G
|
XP_006720911.1:p.Val2302=
|
|
XM_011522381.2:c.6414C>G
|
XP_011520683.1:p.Val2138=
|
|
XM_017022944.1:c.7161C>G
|
XP_016878433.1:p.Val2387=
|
|
NM_004380.3:c.7167C>G
MANE Select
|
NP_004371.2:p.Val2389=
|
|