ENST00000369538.4:c.1332C=
|
ENSP00000358551.4:p.Ile444=
|
|
ENST00000520113.7:c.1344C=
MANE Select
|
ENSP00000430075.3:p.Ile448=
|
|
ENST00000637080.1:c.1127C=
|
ENSP00000489753.1:n.1127C=
|
|
ENST00000639077.1:n.1009C=
|
|
|
ENST00000369538.3:c.1431C=
|
ENSP00000358551.3:p.Ile477=
|
|
ENST00000520113.6:c.1443C=
|
ENSP00000430075.2:p.Ile481=
|
|
NM_000036.2:c.1443C=
|
NP_000027.2:p.Ile481=
|
|
NM_001172626.1:c.1431C=
|
NP_001166097.1:p.Ile477=
|
|
NM_000036.3:c.1344C=
MANE Select
|
NP_000027.3:p.Ile448=
|
|
NM_001172626.2:c.1332C=
|
NP_001166097.2:p.Ile444=
|
|