ENST00000644719.2:c.447G>C
MANE Select
|
ENSP00000496625.1:p.Glu149Asp
|
|
ENST00000418967.6:c.447G>C
|
ENSP00000408860.2:p.Glu149Asp
|
|
ENST00000435122.3:c.357G>C
|
ENSP00000415043.2:p.Glu119Asp
|
|
ENST00000462278.1:n.35G>C
|
|
|
ENST00000464325.5:n.368G>C
|
|
|
ENST00000466779.5:c.*139G>C
|
ENSP00000417321.1:n.*139G>C
|
|
ENST00000466879.5:n.498G>C
|
|
|
ENST00000469053.5:c.*139G>C
|
ENSP00000418104.1:n.*139G>C
|
|
ENST00000471671.4:c.447G>C
|
ENSP00000418561.1:p.Glu149Asp
|
|
ENST00000478281.5:c.480G>C
|
ENSP00000419572.1:p.Glu160Asp
|
|
ENST00000479074.5:n.505G>C
|
|
|
ENST00000479730.5:n.602G>C
|
|
|
ENST00000483041.5:n.616G>C
|
|
|
ENST00000486063.5:n.627G>C
|
|
|
ENST00000488465.1:n.455G>C
|
|
|
NM_000500.7:c.447G>C
|
NP_000491.4:p.Glu149Asp
|
|
NM_001128590.3:c.357G>C
|
NP_001122062.3:p.Glu119Asp
|
|
XM_011514314.1:c.42G>C
|
XP_011512616.1:p.Glu14Asp
|
|
NM_000500.9:c.447G>C
MANE Select
|
NP_000491.4:p.Glu149Asp
|
|
NM_001368143.1:c.42G>C
|
NP_001355072.1:p.Glu14Asp
|
|
NM_001368144.1:c.42G>C
|
NP_001355073.1:p.Glu14Asp
|
|
NM_001128590.4:c.357G>C
|
NP_001122062.3:p.Glu119Asp
|
|
NM_001368143.2:c.42G>C
|
NP_001355072.1:p.Glu14Asp
|
|
NM_001368144.2:c.42G>C
|
NP_001355073.1:p.Glu14Asp
|
|