ENST00000274576.9:c.870C>T
MANE Select
|
ENSP00000274576.5:p.Thr290=
|
|
ENST00000274576.8:c.870C>T
|
ENSP00000274576.4:p.Thr290=
|
|
ENST00000455880.2:c.870C>T
|
ENSP00000411593.2:p.Thr290=
|
|
ENST00000462581.6:c.*628C>T
|
ENSP00000430595.1:n.*628C>T
|
|
ENST00000471351.2:n.1153C>T
|
|
|
NM_000171.3:c.870C>T
|
NP_000162.2:p.Thr290=
|
|
NM_001146040.1:c.870C>T
|
NP_001139512.1:p.Thr290=
|
|
NM_001292000.1:c.621C>T
|
NP_001278929.1:p.Thr207=
|
|
XM_005268412.2:c.870C>T
|
XP_005268469.1:p.Thr290=
|
|
NM_000171.4:c.870C>T
MANE Select
|
NP_000162.2:p.Thr290=
|
|
NM_001146040.2:c.870C>T
|
NP_001139512.1:p.Thr290=
|
|
NM_001292000.2:c.621C>T
|
NP_001278929.1:p.Thr207=
|
|