ENST00000262367.10:c.5553C>G
MANE Select
|
ENSP00000262367.5:p.Arg1851=
|
|
ENST00000262367.9:c.5553C>G
|
ENSP00000262367.5:p.Arg1851=
|
|
ENST00000382070.7:c.5439C>G
|
ENSP00000371502.3:p.Arg1813=
|
|
NM_001079846.1:c.5439C>G
|
NP_001073315.1:p.Arg1813=
|
|
NM_004380.2:c.5553C>G
|
NP_004371.2:p.Arg1851=
|
|
XM_005255124.3:c.5508C>G
|
XP_005255181.1:p.Arg1836=
|
|
XM_005255125.3:c.5136C>G
|
XP_005255182.1:p.Arg1712=
|
|
XM_006720848.2:c.5292C>G
|
XP_006720911.1:p.Arg1764=
|
|
XM_011522380.1:c.5499C>G
|
XP_011520682.1:p.Arg1833=
|
|
XM_011522381.1:c.4800C>G
|
XP_011520683.1:p.Arg1600=
|
|
XM_005255124.4:c.5508C>G
|
XP_005255181.1:p.Arg1836=
|
|
XM_005255125.4:c.5136C>G
|
XP_005255182.1:p.Arg1712=
|
|
XM_006720848.3:c.5292C>G
|
XP_006720911.1:p.Arg1764=
|
|
XM_011522381.2:c.4800C>G
|
XP_011520683.1:p.Arg1600=
|
|
XM_017022944.1:c.5547C>G
|
XP_016878433.1:p.Arg1849=
|
|
NM_004380.3:c.5553C>G
MANE Select
|
NP_004371.2:p.Arg1851=
|
|