ENST00000262367.10:c.6981C>G
MANE Select
|
ENSP00000262367.5:p.Ala2327=
|
|
ENST00000262367.9:c.6981C>G
|
ENSP00000262367.5:p.Ala2327=
|
|
ENST00000382070.7:c.6867C>G
|
ENSP00000371502.3:p.Ala2289=
|
|
NM_001079846.1:c.6867C>G
|
NP_001073315.1:p.Ala2289=
|
|
NM_004380.2:c.6981C>G
|
NP_004371.2:p.Ala2327=
|
|
XM_005255124.3:c.6936C>G
|
XP_005255181.1:p.Ala2312=
|
|
XM_005255125.3:c.6564C>G
|
XP_005255182.1:p.Ala2188=
|
|
XM_006720848.2:c.6720C>G
|
XP_006720911.1:p.Ala2240=
|
|
XM_011522380.1:c.6927C>G
|
XP_011520682.1:p.Ala2309=
|
|
XM_011522381.1:c.6228C>G
|
XP_011520683.1:p.Ala2076=
|
|
XM_005255124.4:c.6936C>G
|
XP_005255181.1:p.Ala2312=
|
|
XM_005255125.4:c.6564C>G
|
XP_005255182.1:p.Ala2188=
|
|
XM_006720848.3:c.6720C>G
|
XP_006720911.1:p.Ala2240=
|
|
XM_011522381.2:c.6228C>G
|
XP_011520683.1:p.Ala2076=
|
|
XM_017022944.1:c.6975C>G
|
XP_016878433.1:p.Ala2325=
|
|
NM_004380.3:c.6981C>G
MANE Select
|
NP_004371.2:p.Ala2327=
|
|