ENST00000644719.2:c.1063C>A
MANE Select
|
ENSP00000496625.1:p.Arg355Ser
|
|
ENST00000418967.6:c.1063C>A
|
ENSP00000408860.2:p.Arg355Ser
|
|
ENST00000435122.3:c.973C>A
|
ENSP00000415043.2:p.Arg325Ser
|
|
ENST00000479074.5:n.1121C>A
|
|
|
ENST00000479730.5:n.1179C>A
|
|
|
ENST00000483041.5:n.1232C>A
|
|
|
ENST00000486063.5:n.1042C>A
|
|
|
NM_000500.7:c.1063C>A
|
NP_000491.4:p.Arg355Ser
|
|
NM_001128590.3:c.973C>A
|
NP_001122062.3:p.Arg325Ser
|
|
XM_011514314.1:c.658C>A
|
XP_011512616.1:p.Arg220Ser
|
|
NM_000500.9:c.1063C>A
MANE Select
|
NP_000491.4:p.Arg355Ser
|
|
NM_001368143.1:c.658C>A
|
NP_001355072.1:p.Arg220Ser
|
|
NM_001368144.1:c.658C>A
|
NP_001355073.1:p.Arg220Ser
|
|
NM_001128590.4:c.973C>A
|
NP_001122062.3:p.Arg325Ser
|
|
NM_001368143.2:c.658C>A
|
NP_001355072.1:p.Arg220Ser
|
|
NM_001368144.2:c.658C>A
|
NP_001355073.1:p.Arg220Ser
|
|