ENST00000644719.2:c.1054G=
MANE Select
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ENSP00000496625.1:p.Glu352=
|
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ENST00000418967.6:c.1054G=
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ENSP00000408860.2:p.Glu352=
|
|
ENST00000435122.3:c.964G=
|
ENSP00000415043.2:p.Glu322=
|
|
ENST00000479074.5:n.1112G=
|
|
|
ENST00000479730.5:n.1170G=
|
|
|
ENST00000483041.5:n.1223G=
|
|
|
ENST00000486063.5:n.1033G=
|
|
|
NM_000500.7:c.1054G=
|
NP_000491.4:p.Glu352=
|
|
NM_001128590.3:c.964G=
|
NP_001122062.3:p.Glu322=
|
|
XM_011514314.1:c.649G=
|
XP_011512616.1:p.Glu217=
|
|
NM_000500.9:c.1054G=
MANE Select
|
NP_000491.4:p.Glu352=
|
|
NM_001368143.1:c.649G=
|
NP_001355072.1:p.Glu217=
|
|
NM_001368144.1:c.649G=
|
NP_001355073.1:p.Glu217=
|
|
NM_001128590.4:c.964G=
|
NP_001122062.3:p.Glu322=
|
|
NM_001368143.2:c.649G=
|
NP_001355072.1:p.Glu217=
|
|
NM_001368144.2:c.649G=
|
NP_001355073.1:p.Glu217=
|
|