ENST00000367049.9:c.753C>T
MANE Select
|
ENSP00000356016.4:p.Asp251=
|
|
ENST00000367051.6:c.487+12222C>T
|
ENSP00000356018.1:n.487+12222C>T
|
|
ENST00000367052.6:c.753C>T
|
ENSP00000356019.1:p.Asp251=
|
|
ENST00000367053.6:c.753C>T
|
ENSP00000356020.1:p.Asp251=
|
|
ENST00000400960.7:c.753C>T
|
ENSP00000383744.2:p.Asp251=
|
|
ENST00000367049.8:c.753C>T
|
ENSP00000356016.4:p.Asp251=
|
|
ENST00000367050.8:n.874C>T
|
|
|
ENST00000367051.5:c.487+12222C>T
|
ENSP00000356018.1:n.487+12222C>T
|
|
ENST00000367052.5:c.753C>T
|
ENSP00000356019.1:p.Asp251=
|
|
ENST00000367053.5:c.753C>T
|
ENSP00000356020.1:p.Asp251=
|
|
ENST00000400960.6:c.753C>T
|
ENSP00000383744.2:p.Asp251=
|
|
ENST00000434033.5:n.680C>T
|
|
|
ENST00000436595.1:n.414+12222C>T
|
|
|
ENST00000450439.5:n.680C>T
|
|
|
ENST00000529814.1:c.680C>T
|
|
|
ENST00000534202.5:c.753C>T
|
ENSP00000436139.2:p.Asp251=
|
|
NM_000573.3:c.753C>T
|
NP_000564.2:p.Asp251=
|
|
NM_000651.4:c.753C>T
|
NP_000642.3:p.Asp251=
|
|
XM_006711166.2:c.768C>T
|
XP_006711229.1:p.Asp256=
|
|
XM_011509205.1:c.768C>T
|
XP_011507507.1:p.Asp256=
|
|
NM_000651.5:c.753C>T
|
NP_000642.3:p.Asp251=
|
|
XM_024453287.1:c.768C>T
|
XP_024309055.1:p.Asp256=
|
|
NM_000573.4:c.753C>T
|
NP_000564.2:p.Asp251=
|
|
NM_000651.6:c.753C>T
MANE Select
|
NP_000642.3:p.Asp251=
|
|