ENST00000262367.10:c.5572C=
MANE Select
|
ENSP00000262367.5:p.Arg1858=
|
|
ENST00000262367.9:c.5572C=
|
ENSP00000262367.5:p.Arg1858=
|
|
ENST00000382070.7:c.5458C=
|
ENSP00000371502.3:p.Arg1820=
|
|
NM_001079846.1:c.5458C=
|
NP_001073315.1:p.Arg1820=
|
|
NM_004380.2:c.5572C=
|
NP_004371.2:p.Arg1858=
|
|
XM_005255124.3:c.5527C=
|
XP_005255181.1:p.Arg1843=
|
|
XM_005255125.3:c.5155C=
|
XP_005255182.1:p.Arg1719=
|
|
XM_006720848.2:c.5311C=
|
XP_006720911.1:p.Arg1771=
|
|
XM_011522380.1:c.5518C=
|
XP_011520682.1:p.Arg1840=
|
|
XM_011522381.1:c.4819C=
|
XP_011520683.1:p.Arg1607=
|
|
XM_005255124.4:c.5527C=
|
XP_005255181.1:p.Arg1843=
|
|
XM_005255125.4:c.5155C=
|
XP_005255182.1:p.Arg1719=
|
|
XM_006720848.3:c.5311C=
|
XP_006720911.1:p.Arg1771=
|
|
XM_011522381.2:c.4819C=
|
XP_011520683.1:p.Arg1607=
|
|
XM_017022944.1:c.5566C=
|
XP_016878433.1:p.Arg1856=
|
|
NM_004380.3:c.5572C=
MANE Select
|
NP_004371.2:p.Arg1858=
|
|