ENST00000219548.9:c.478G=
(STUB1)
MANE Select
|
ENSP00000219548.4:p.Glu160=
|
|
ENST00000219548.8:c.478G=
(STUB1)
|
ENSP00000219548.4:p.Glu160=
|
|
ENST00000563505.5:n.574G=
(STUB1)
|
|
|
ENST00000564316.1:c.77G=
(STUB1)
|
|
|
ENST00000564370.5:c.262G=
(STUB1)
|
ENSP00000456875.1:p.Glu88=
|
|
ENST00000565677.5:c.262G=
(STUB1)
|
ENSP00000457228.1:p.Glu88=
|
|
ENST00000566181.2:n.247G=
(STUB1)
|
|
|
ENST00000566408.5:c.195G=
(STUB1)
|
|
|
ENST00000567173.5:c.421G=
(STUB1)
|
ENSP00000456591.1:p.Glu141=
|
|
ENST00000569248.5:n.1052G=
(STUB1)
|
|
|
ENST00000620831.4:c.-50+38254G=
(MSLN)
|
ENSP00000482893.1:n.-50+38254G=
|
|
NM_001293197.1:c.262G=
(STUB1)
|
NP_001280126.1:p.Glu88=
|
|
NM_005861.3:c.478G=
(STUB1)
|
NP_005852.2:p.Glu160=
|
|
NM_005861.4:c.478G=
(STUB1)
MANE Select
|
NP_005852.2:p.Glu160=
|
|
NM_001293197.2:c.262G=
(STUB1)
|
NP_001280126.1:p.Glu88=
|
|