ENST00000225737.11:c.1890C>T
MANE Select
|
ENSP00000225737.6:p.Ala630=
|
|
ENST00000225737.10:c.1890C>T
|
ENSP00000225737.6:p.Ala630=
|
|
ENST00000395536.7:c.1716C>T
|
ENSP00000378907.3:p.Ala572=
|
|
ENST00000578898.1:c.317C>T
|
|
|
ENST00000583951.1:c.201C>T
|
ENSP00000463398.1:p.Ala67=
|
|
NM_007202.3:c.1890C>T
|
NP_009133.2:p.Ala630=
|
|
XM_006721431.2:c.1835-3042C>T
|
XP_006721494.1:n.1835-3042C>T
|
|
XM_006721432.2:c.1716C>T
|
XP_006721495.1:p.Ala572=
|
|
XR_933969.1:n.1938C>T
|
|
|
XR_933970.1:n.1883-3042C>T
|
|
|
NM_001330152.1:c.1716C>T
|
NP_001317081.1:p.Ala572=
|
|
XR_001752418.2:n.2002C>T
|
|
|
XR_933969.3:n.1921C>T
|
|
|
NM_007202.4:c.1890C>T
MANE Select
|
NP_009133.2:p.Ala630=
|
|
NM_001330152.2:c.1716C>T
|
NP_001317081.1:p.Ala572=
|
|