ENST00000352480.10:c.816C>T
MANE Select
|
ENSP00000253004.6:p.Arg272=
|
|
ENST00000352480.9:c.816C>T
|
ENSP00000253004.6:p.Arg272=
|
|
ENST00000372386.6:n.87C>T
|
|
|
ENST00000372393.7:c.816C>T
|
ENSP00000361469.2:p.Arg272=
|
|
ENST00000372394.5:c.816C>T
|
ENSP00000361471.1:p.Arg272=
|
|
ENST00000470849.4:n.541C>T
|
|
|
ENST00000492400.5:n.325C>T
|
|
|
ENST00000493984.6:n.593C>T
|
|
|
NM_000050.4:c.816C>T
|
NP_000041.2:p.Arg272=
|
|
NM_054012.3:c.816C>T
|
NP_446464.1:p.Arg272=
|
|
XM_005272200.2:c.816C>T
|
XP_005272257.1:p.Arg272=
|
|
XM_011518705.1:c.930C>T
|
XP_011517007.1:p.Arg310=
|
|
XM_005272200.3:c.816C>T
|
XP_005272257.1:p.Arg272=
|
|
XM_011518705.2:c.930C>T
|
XP_011517007.1:p.Arg310=
|
|
XM_017014729.1:c.912C>T
|
XP_016870218.1:p.Arg304=
|
|
NM_054012.4:c.816C>T
MANE Select
|
NP_446464.1:p.Arg272=
|
|