ENST00000262367.10:c.5565C>A
MANE Select
|
ENSP00000262367.5:p.Ile1855=
|
|
ENST00000262367.9:c.5565C>A
|
ENSP00000262367.5:p.Ile1855=
|
|
ENST00000382070.7:c.5451C>A
|
ENSP00000371502.3:p.Ile1817=
|
|
NM_001079846.1:c.5451C>A
|
NP_001073315.1:p.Ile1817=
|
|
NM_004380.2:c.5565C>A
|
NP_004371.2:p.Ile1855=
|
|
XM_005255124.3:c.5520C>A
|
XP_005255181.1:p.Ile1840=
|
|
XM_005255125.3:c.5148C>A
|
XP_005255182.1:p.Ile1716=
|
|
XM_006720848.2:c.5304C>A
|
XP_006720911.1:p.Ile1768=
|
|
XM_011522380.1:c.5511C>A
|
XP_011520682.1:p.Ile1837=
|
|
XM_011522381.1:c.4812C>A
|
XP_011520683.1:p.Ile1604=
|
|
XM_005255124.4:c.5520C>A
|
XP_005255181.1:p.Ile1840=
|
|
XM_005255125.4:c.5148C>A
|
XP_005255182.1:p.Ile1716=
|
|
XM_006720848.3:c.5304C>A
|
XP_006720911.1:p.Ile1768=
|
|
XM_011522381.2:c.4812C>A
|
XP_011520683.1:p.Ile1604=
|
|
XM_017022944.1:c.5559C>A
|
XP_016878433.1:p.Ile1853=
|
|
NM_004380.3:c.5565C>A
MANE Select
|
NP_004371.2:p.Ile1855=
|
|