ENST00000376649.8:c.783C>T
MANE Select
|
ENSP00000365837.3:p.Arg261=
|
|
ENST00000322060.9:c.699C>T
|
ENSP00000324726.5:p.Arg233=
|
|
ENST00000376649.7:c.783C>T
|
ENSP00000365837.3:p.Arg261=
|
|
ENST00000443358.6:c.699C>T
|
ENSP00000392451.2:p.Arg233=
|
|
ENST00000535067.5:c.358-2009C>T
|
ENSP00000443969.1:n.358-2009C>T
|
|
ENST00000542167.2:c.624C>T
|
ENSP00000438948.1:p.Arg208=
|
|
ENST00000543754.1:n.604C>T
|
|
|
NM_001002019.2:c.699C>T
|
NP_001002019.1:p.Arg233=
|
|
NM_001002020.2:c.699C>T
|
NP_001002020.1:p.Arg233=
|
|
NM_025215.5:c.783C>T
|
NP_079491.2:p.Arg261=
|
|
XM_011538768.1:c.384C>T
|
XP_011537070.1:p.Arg128=
|
|
XM_011538768.3:c.384C>T
|
XP_011537070.1:p.Arg128=
|
|
XR_001748872.1:n.1238C>T
|
|
|
NM_001002019.3:c.699C>T
|
NP_001002019.1:p.Arg233=
|
|
NM_001002020.3:c.699C>T
|
NP_001002020.1:p.Arg233=
|
|
NM_025215.6:c.783C>T
MANE Select
|
NP_079491.2:p.Arg261=
|
|