ENST00000302804.12:c.642A>G
MANE Select
|
ENSP00000302898.6:p.Arg214=
|
|
ENST00000302804.11:c.642A>G
|
ENSP00000302898.6:p.Arg214=
|
|
ENST00000415300.6:c.585A>G
|
ENSP00000407162.1:p.Arg195=
|
|
ENST00000448930.5:c.537A>G
|
ENSP00000406798.2:p.Arg179=
|
|
ENST00000594599.1:c.126A>G
|
ENSP00000469894.1:p.Arg42=
|
|
ENST00000596375.1:c.*203A>G
|
ENSP00000470465.1:n.*203A>G
|
|
ENST00000598785.5:c.540A>G
|
ENSP00000471830.1:p.Arg180=
|
|
ENST00000599062.5:c.633A>G
|
ENSP00000469983.1:p.Arg211=
|
|
ENST00000601799.5:c.*941A>G
|
ENSP00000468918.1:n.*941A>G
|
|
NM_001015878.1:c.642A>G
|
NP_001015878.1:p.Arg214=
|
|
NM_001015879.1:c.585A>G
|
NP_001015879.1:p.Arg195=
|
|
NM_003160.2:c.540A>G
|
NP_003151.2:p.Arg180=
|
|
XR_430209.2:n.1536A>G
|
|
|
XR_430209.3:n.1579A>G
|
|
|
NM_001015878.2:c.642A>G
MANE Select
|
NP_001015878.1:p.Arg214=
|
|
NM_001015879.2:c.585A>G
|
NP_001015879.1:p.Arg195=
|
|
NM_003160.3:c.540A>G
|
NP_003151.2:p.Arg180=
|
|