ENST00000264595.7:c.505A>C
MANE Select
|
ENSP00000264595.2:p.Arg169=
|
|
ENST00000264595.6:c.505A>C
|
ENSP00000264595.2:p.Arg169=
|
|
ENST00000502310.5:c.160A>C
|
ENSP00000423798.1:p.Arg54=
|
|
ENST00000506853.5:n.539A>C
|
|
|
ENST00000510635.1:c.201A>C
|
|
|
ENST00000510955.5:n.426A>C
|
|
|
NM_000027.3:c.505A>C
|
NP_000018.2:p.Arg169=
|
|
NM_001171988.1:c.505A>C
|
NP_001165459.1:p.Arg169=
|
|
NR_033655.1:n.633A>C
|
|
|
XM_006714123.2:c.505A>C
|
XP_006714186.1:p.Arg169=
|
|
XR_001741155.2:n.599A>C
|
|
|
NM_000027.4:c.505A>C
MANE Select
|
NP_000018.2:p.Arg169=
|
|
NM_001171988.2:c.505A>C
|
NP_001165459.1:p.Arg169=
|
|
NR_033655.2:n.567A>C
|
|
|