ENST00000644719.2:c.423G>C
MANE Select
|
ENSP00000496625.1:p.Glu141Asp
|
|
ENST00000418967.6:c.423G>C
|
ENSP00000408860.2:p.Glu141Asp
|
|
ENST00000435122.3:c.333G>C
|
ENSP00000415043.2:p.Glu111Asp
|
|
ENST00000462278.1:n.11G>C
|
|
|
ENST00000464325.5:n.344G>C
|
|
|
ENST00000466779.5:c.*115G>C
|
ENSP00000417321.1:n.*115G>C
|
|
ENST00000466879.5:n.474G>C
|
|
|
ENST00000469053.5:c.*115G>C
|
ENSP00000418104.1:n.*115G>C
|
|
ENST00000471671.4:c.423G>C
|
ENSP00000418561.1:p.Glu141Asp
|
|
ENST00000478281.5:c.456G>C
|
ENSP00000419572.1:p.Glu152Asp
|
|
ENST00000479074.5:n.481G>C
|
|
|
ENST00000479730.5:n.578G>C
|
|
|
ENST00000483041.5:n.592G>C
|
|
|
ENST00000486063.5:n.603G>C
|
|
|
ENST00000488465.1:n.431G>C
|
|
|
NM_000500.7:c.423G>C
|
NP_000491.4:p.Glu141Asp
|
|
NM_001128590.3:c.333G>C
|
NP_001122062.3:p.Glu111Asp
|
|
XM_011514314.1:c.18G>C
|
XP_011512616.1:p.Glu6Asp
|
|
NM_000500.9:c.423G>C
MANE Select
|
NP_000491.4:p.Glu141Asp
|
|
NM_001368143.1:c.18G>C
|
NP_001355072.1:p.Glu6Asp
|
|
NM_001368144.1:c.18G>C
|
NP_001355073.1:p.Glu6Asp
|
|
NM_001128590.4:c.333G>C
|
NP_001122062.3:p.Glu111Asp
|
|
NM_001368143.2:c.18G>C
|
NP_001355072.1:p.Glu6Asp
|
|
NM_001368144.2:c.18G>C
|
NP_001355073.1:p.Glu6Asp
|
|