ENST00000262367.10:c.5568G>A
MANE Select
|
ENSP00000262367.5:p.Gln1856=
|
|
ENST00000262367.9:c.5568G>A
|
ENSP00000262367.5:p.Gln1856=
|
|
ENST00000382070.7:c.5454G>A
|
ENSP00000371502.3:p.Gln1818=
|
|
NM_001079846.1:c.5454G>A
|
NP_001073315.1:p.Gln1818=
|
|
NM_004380.2:c.5568G>A
|
NP_004371.2:p.Gln1856=
|
|
XM_005255124.3:c.5523G>A
|
XP_005255181.1:p.Gln1841=
|
|
XM_005255125.3:c.5151G>A
|
XP_005255182.1:p.Gln1717=
|
|
XM_006720848.2:c.5307G>A
|
XP_006720911.1:p.Gln1769=
|
|
XM_011522380.1:c.5514G>A
|
XP_011520682.1:p.Gln1838=
|
|
XM_011522381.1:c.4815G>A
|
XP_011520683.1:p.Gln1605=
|
|
XM_005255124.4:c.5523G>A
|
XP_005255181.1:p.Gln1841=
|
|
XM_005255125.4:c.5151G>A
|
XP_005255182.1:p.Gln1717=
|
|
XM_006720848.3:c.5307G>A
|
XP_006720911.1:p.Gln1769=
|
|
XM_011522381.2:c.4815G>A
|
XP_011520683.1:p.Gln1605=
|
|
XM_017022944.1:c.5562G>A
|
XP_016878433.1:p.Gln1854=
|
|
NM_004380.3:c.5568G>A
MANE Select
|
NP_004371.2:p.Gln1856=
|
|