ENST00000381129.8:c.1116A>T
MANE Select
|
ENSP00000370521.3:p.Thr372=
|
|
ENST00000250087.9:c.927A>T
|
ENSP00000250087.5:p.Thr309=
|
|
ENST00000381128.2:c.*988A>T
|
ENSP00000370520.2:n.*988A>T
|
|
ENST00000381129.7:c.1116A>T
|
ENSP00000370521.3:p.Thr372=
|
|
ENST00000570466.5:c.1050A>T
|
ENSP00000461287.1:p.Thr350=
|
|
ENST00000570584.5:c.251+8420A>T
|
|
|
ENST00000574506.5:c.1080A>T
|
ENSP00000458456.1:p.Thr360=
|
|
ENST00000575265.5:c.*1087A>T
|
ENSP00000459673.1:n.*1087A>T
|
|
ENST00000576307.5:c.936A>T
|
ENSP00000459522.1:p.Thr312=
|
|
ENST00000576776.5:c.1044A>T
|
ENSP00000460827.1:p.Thr348=
|
|
ENST00000621374.4:c.*134A>T
|
ENSP00000481337.1:n.*134A>T
|
|
NM_001033054.2:c.927A>T
|
NP_001028226.1:p.Thr309=
|
|
NM_001033055.2:c.936A>T
|
NP_001028227.1:p.Thr312=
|
|
NM_001285399.2:c.1080A>T
|
NP_001272328.1:p.Thr360=
|
|
NM_001285400.2:c.1050A>T
|
NP_001272329.1:p.Thr350=
|
|
NM_001285401.2:c.1044A>T
|
NP_001272330.1:p.Thr348=
|
|
NM_001285402.1:c.999A>T
|
NP_001272331.1:p.Thr333=
|
|
NM_014336.4:c.1116A>T
|
NP_055151.3:p.Thr372=
|
|
NM_001033054.3:c.927A>T
|
NP_001028226.1:p.Thr309=
|
|
NM_001033055.3:c.936A>T
|
NP_001028227.1:p.Thr312=
|
|
NM_001285399.3:c.1080A>T
|
NP_001272328.1:p.Thr360=
|
|
NM_001285400.3:c.1050A>T
|
NP_001272329.1:p.Thr350=
|
|
NM_001285401.3:c.1044A>T
|
NP_001272330.1:p.Thr348=
|
|
NM_001285402.2:c.999A>T
|
NP_001272331.1:p.Thr333=
|
|
NM_001285403.3:c.*1087A>T
|
NP_001272332.1:n.*1087A>T
|
|
NM_014336.5:c.1116A>T
MANE Select
|
NP_055151.3:p.Thr372=
|
|
NM_001285403.4:c.*1087A>T
|
NP_001272332.1:n.*1087A>T
|
|