ENST00000644719.2:c.422A=
MANE Select
|
ENSP00000496625.1:p.Glu141=
|
|
ENST00000418967.6:c.422A=
|
ENSP00000408860.2:p.Glu141=
|
|
ENST00000435122.3:c.332A=
|
ENSP00000415043.2:p.Glu111=
|
|
ENST00000462278.1:n.10A=
|
|
|
ENST00000464325.5:n.343A=
|
|
|
ENST00000466779.5:c.*114A=
|
ENSP00000417321.1:n.*114A=
|
|
ENST00000466879.5:n.473A=
|
|
|
ENST00000469053.5:c.*114A=
|
ENSP00000418104.1:n.*114A=
|
|
ENST00000471671.4:c.422A=
|
ENSP00000418561.1:p.Glu141=
|
|
ENST00000478281.5:c.455A=
|
ENSP00000419572.1:p.Glu152=
|
|
ENST00000479074.5:n.480A=
|
|
|
ENST00000479730.5:n.577A=
|
|
|
ENST00000483041.5:n.591A=
|
|
|
ENST00000486063.5:n.602A=
|
|
|
ENST00000488465.1:n.430A=
|
|
|
NM_000500.7:c.422A=
|
NP_000491.4:p.Glu141=
|
|
NM_001128590.3:c.332A=
|
NP_001122062.3:p.Glu111=
|
|
XM_011514314.1:c.17A=
|
XP_011512616.1:p.Glu6=
|
|
NM_000500.9:c.422A=
MANE Select
|
NP_000491.4:p.Glu141=
|
|
NM_001368143.1:c.17A=
|
NP_001355072.1:p.Glu6=
|
|
NM_001368144.1:c.17A=
|
NP_001355073.1:p.Glu6=
|
|
NM_001128590.4:c.332A=
|
NP_001122062.3:p.Glu111=
|
|
NM_001368143.2:c.17A=
|
NP_001355072.1:p.Glu6=
|
|
NM_001368144.2:c.17A=
|
NP_001355073.1:p.Glu6=
|
|