ENST00000296585.10:c.916A>C
MANE Select
|
ENSP00000296585.5:p.Arg306=
|
|
ENST00000296585.9:c.916A>C
|
ENSP00000296585.5:p.Arg306=
|
|
ENST00000503810.6:c.*260A>C
|
ENSP00000426489.1:n.*260A>C
|
|
ENST00000509814.5:c.916A>C
|
ENSP00000424397.1:p.Arg306=
|
|
ENST00000509960.5:c.916A>C
|
ENSP00000424642.1:p.Arg306=
|
|
ENST00000510722.1:c.916A>C
|
ENSP00000422145.1:p.Arg306=
|
|
ENST00000513685.5:c.*630A>C
|
ENSP00000422095.1:n.*630A>C
|
|
NM_002203.3:c.916A>C
|
NP_002194.2:p.Arg306=
|
|
NR_073103.1:n.1059A>C
|
|
|
NR_073104.1:n.1059A>C
|
|
|
NR_073105.1:n.1059A>C
|
|
|
NR_073106.1:n.1059A>C
|
|
|
NR_073107.1:n.938A>C
|
|
|
NM_002203.4:c.916A>C
MANE Select
|
NP_002194.2:p.Arg306=
|
|
NR_073103.2:n.1033A>C
|
|
|
NR_073104.2:n.1033A>C
|
|
|
NR_073105.2:n.1033A>C
|
|
|
NR_073106.2:n.1033A>C
|
|
|
NR_073107.2:n.912A>C
|
|
|