ENST00000328300.11:c.4128A>C
MANE Select
|
ENSP00000331902.7:p.Ile1376=
|
|
ENST00000361603.7:c.4110A>C
|
ENSP00000354505.2:p.Ile1370=
|
|
ENST00000510690.2:n.622A>C
|
|
|
ENST00000328300.10:c.4128A>C
|
ENSP00000331902.6:p.Ile1376=
|
|
ENST00000361603.6:c.4110A>C
|
ENSP00000354505.2:p.Ile1370=
|
|
ENST00000489230.1:n.531A>C
|
|
|
NM_000495.4:c.4110A>C
|
NP_000486.1:p.Ile1370=
|
|
NM_033380.2:c.4128A>C
|
NP_203699.1:p.Ile1376=
|
|
XM_005262070.2:c.4119A>C
|
XP_005262127.1:p.Ile1373=
|
|
XM_006724616.2:c.4128A>C
|
XP_006724679.1:p.Ile1376=
|
|
XM_011530849.1:c.3804A>C
|
XP_011529151.1:p.Ile1268=
|
|
XM_011530851.1:c.1701A>C
|
XP_011529153.1:p.Ile567=
|
|
XM_011530849.2:c.4143A>C
|
XP_011529151.2:p.Ile1381=
|
|
XM_017029259.2:c.4134A>C
|
XP_016884748.1:p.Ile1378=
|
|
XM_017029260.1:c.4125A>C
|
XP_016884749.1:p.Ile1375=
|
|
XM_017029263.2:c.2463A>C
|
XP_016884752.1:p.Ile821=
|
|
NM_000495.5:c.4110A>C
|
NP_000486.1:p.Ile1370=
|
|
NM_033380.3:c.4128A>C
MANE Select
|
NP_203699.1:p.Ile1376=
|
|