ENST00000262367.10:c.7317G=
MANE Select
|
ENSP00000262367.5:p.Val2439=
|
|
ENST00000262367.9:c.7317G=
|
ENSP00000262367.5:p.Val2439=
|
|
ENST00000382070.7:c.7203G=
|
ENSP00000371502.3:p.Val2401=
|
|
NM_001079846.1:c.7203G=
|
NP_001073315.1:p.Val2401=
|
|
NM_004380.2:c.7317G=
|
NP_004371.2:p.Val2439=
|
|
XM_005255124.3:c.7272G=
|
XP_005255181.1:p.Val2424=
|
|
XM_005255125.3:c.6900G=
|
XP_005255182.1:p.Val2300=
|
|
XM_006720848.2:c.7056G=
|
XP_006720911.1:p.Val2352=
|
|
XM_011522380.1:c.7263G=
|
XP_011520682.1:p.Val2421=
|
|
XM_011522381.1:c.6564G=
|
XP_011520683.1:p.Val2188=
|
|
XM_005255124.4:c.7272G=
|
XP_005255181.1:p.Val2424=
|
|
XM_005255125.4:c.6900G=
|
XP_005255182.1:p.Val2300=
|
|
XM_006720848.3:c.7056G=
|
XP_006720911.1:p.Val2352=
|
|
XM_011522381.2:c.6564G=
|
XP_011520683.1:p.Val2188=
|
|
XM_017022944.1:c.7311G=
|
XP_016878433.1:p.Val2437=
|
|
NM_004380.3:c.7317G=
MANE Select
|
NP_004371.2:p.Val2439=
|
|