ENST00000644719.2:c.939G>T
MANE Select
|
ENSP00000496625.1:p.Glu313Asp
|
|
ENST00000418967.6:c.939G>T
|
ENSP00000408860.2:p.Glu313Asp
|
|
ENST00000435122.3:c.849G>T
|
ENSP00000415043.2:p.Glu283Asp
|
|
ENST00000479074.5:n.997G>T
|
|
|
ENST00000479730.5:n.1055G>T
|
|
|
ENST00000483041.5:n.1108G>T
|
|
|
ENST00000486063.5:n.919-201G>T
|
|
|
NM_000500.7:c.939G>T
|
NP_000491.4:p.Glu313Asp
|
|
NM_001128590.3:c.849G>T
|
NP_001122062.3:p.Glu283Asp
|
|
XM_011514314.1:c.534G>T
|
XP_011512616.1:p.Glu178Asp
|
|
NM_000500.9:c.939G>T
MANE Select
|
NP_000491.4:p.Glu313Asp
|
|
NM_001368143.1:c.534G>T
|
NP_001355072.1:p.Glu178Asp
|
|
NM_001368144.1:c.534G>T
|
NP_001355073.1:p.Glu178Asp
|
|
NM_001128590.4:c.849G>T
|
NP_001122062.3:p.Glu283Asp
|
|
NM_001368143.2:c.534G>T
|
NP_001355072.1:p.Glu178Asp
|
|
NM_001368144.2:c.534G>T
|
NP_001355073.1:p.Glu178Asp
|
|