ENST00000276297.9:c.1845C>T
MANE Select
|
ENSP00000276297.4:p.Thr615=
|
|
ENST00000276297.8:c.1845C>T
|
ENSP00000276297.4:p.Thr615=
|
|
ENST00000358919.6:c.534C>T
|
ENSP00000351797.2:p.Thr178=
|
|
ENST00000510250.2:n.414C>T
|
|
|
ENST00000512044.6:c.636C>T
|
ENSP00000422595.2:p.Thr212=
|
|
ENST00000520226.5:c.312C>T
|
ENSP00000428028.1:p.Thr104=
|
|
NM_001164271.1:c.312C>T
|
NP_001157743.1:p.Thr104=
|
|
NM_001316668.1:c.636C>T
|
NP_001303597.1:p.Thr212=
|
|
NM_006094.4:c.534C>T
|
NP_006085.2:p.Thr178=
|
|
NM_182643.2:c.1845C>T
|
NP_872584.2:p.Thr615=
|
|
XM_005273374.1:c.1845C>T
|
XP_005273431.1:p.Thr615=
|
|
NM_001348081.1:c.1845C>T
|
NP_001335010.1:p.Thr615=
|
|
NM_001348082.1:c.312C>T
|
NP_001335011.1:p.Thr104=
|
|
NM_001348083.1:c.312C>T
|
NP_001335012.1:p.Thr104=
|
|
NM_001348084.1:c.312C>T
|
NP_001335013.1:p.Thr104=
|
|
NM_182643.3:c.1845C>T
MANE Select
|
NP_872584.2:p.Thr615=
|
|
NM_001316668.2:c.636C>T
|
NP_001303597.1:p.Thr212=
|
|
NM_001348081.2:c.1845C>T
|
NP_001335010.1:p.Thr615=
|
|
NM_001348082.2:c.312C>T
|
NP_001335011.1:p.Thr104=
|
|
NM_001348084.2:c.312C>T
|
NP_001335013.1:p.Thr104=
|
|
NM_006094.5:c.534C>T
|
NP_006085.2:p.Thr178=
|
|
NM_001164271.2:c.312C>T
|
NP_001157743.1:p.Thr104=
|
|