ENST00000262367.10:c.7242C>A
MANE Select
|
ENSP00000262367.5:p.Thr2414=
|
|
ENST00000262367.9:c.7242C>A
|
ENSP00000262367.5:p.Thr2414=
|
|
ENST00000382070.7:c.7128C>A
|
ENSP00000371502.3:p.Thr2376=
|
|
NM_001079846.1:c.7128C>A
|
NP_001073315.1:p.Thr2376=
|
|
NM_004380.2:c.7242C>A
|
NP_004371.2:p.Thr2414=
|
|
XM_005255124.3:c.7197C>A
|
XP_005255181.1:p.Thr2399=
|
|
XM_005255125.3:c.6825C>A
|
XP_005255182.1:p.Thr2275=
|
|
XM_006720848.2:c.6981C>A
|
XP_006720911.1:p.Thr2327=
|
|
XM_011522380.1:c.7188C>A
|
XP_011520682.1:p.Thr2396=
|
|
XM_011522381.1:c.6489C>A
|
XP_011520683.1:p.Thr2163=
|
|
XM_005255124.4:c.7197C>A
|
XP_005255181.1:p.Thr2399=
|
|
XM_005255125.4:c.6825C>A
|
XP_005255182.1:p.Thr2275=
|
|
XM_006720848.3:c.6981C>A
|
XP_006720911.1:p.Thr2327=
|
|
XM_011522381.2:c.6489C>A
|
XP_011520683.1:p.Thr2163=
|
|
XM_017022944.1:c.7236C>A
|
XP_016878433.1:p.Thr2412=
|
|
NM_004380.3:c.7242C>A
MANE Select
|
NP_004371.2:p.Thr2414=
|
|