ENST00000262367.10:c.5931C>T
MANE Select
|
ENSP00000262367.5:p.Ile1977=
|
|
ENST00000262367.9:c.5931C>T
|
ENSP00000262367.5:p.Ile1977=
|
|
ENST00000382070.7:c.5817C>T
|
ENSP00000371502.3:p.Ile1939=
|
|
NM_001079846.1:c.5817C>T
|
NP_001073315.1:p.Ile1939=
|
|
NM_004380.2:c.5931C>T
|
NP_004371.2:p.Ile1977=
|
|
XM_005255124.3:c.5886C>T
|
XP_005255181.1:p.Ile1962=
|
|
XM_005255125.3:c.5514C>T
|
XP_005255182.1:p.Ile1838=
|
|
XM_006720848.2:c.5670C>T
|
XP_006720911.1:p.Ile1890=
|
|
XM_011522380.1:c.5877C>T
|
XP_011520682.1:p.Ile1959=
|
|
XM_011522381.1:c.5178C>T
|
XP_011520683.1:p.Ile1726=
|
|
XM_005255124.4:c.5886C>T
|
XP_005255181.1:p.Ile1962=
|
|
XM_005255125.4:c.5514C>T
|
XP_005255182.1:p.Ile1838=
|
|
XM_006720848.3:c.5670C>T
|
XP_006720911.1:p.Ile1890=
|
|
XM_011522381.2:c.5178C>T
|
XP_011520683.1:p.Ile1726=
|
|
XM_017022944.1:c.5925C>T
|
XP_016878433.1:p.Ile1975=
|
|
NM_004380.3:c.5931C>T
MANE Select
|
NP_004371.2:p.Ile1977=
|
|