ENST00000302850.10:c.4134G>T
MANE Select
|
ENSP00000303830.4:p.Arg1378=
|
|
ENST00000302850.9:c.4134G>T
|
ENSP00000303830.4:p.Arg1378=
|
|
ENST00000341500.9:c.4098G>T
|
ENSP00000342838.4:p.Arg1366=
|
|
NM_000208.2:c.4134G>T
|
NP_000199.2:p.Arg1378=
|
|
NM_000208.3:c.4134G>T
|
NP_000199.2:p.Arg1378=
|
|
NM_001079817.1:c.4098G>T
|
NP_001073285.1:p.Arg1366=
|
|
NM_001079817.2:c.4098G>T
|
NP_001073285.1:p.Arg1366=
|
|
XM_011527988.1:c.4209G>T
|
XP_011526290.1:p.Arg1403=
|
|
XM_011527989.1:c.4173G>T
|
XP_011526291.1:p.Arg1391=
|
|
XM_011527988.2:c.4131G>T
|
XP_011526290.2:p.Arg1377=
|
|
XM_011527989.3:c.4095G>T
|
XP_011526291.2:p.Arg1365=
|
|
NM_000208.4:c.4134G>T
MANE Select
|
NP_000199.2:p.Arg1378=
|
|
NM_001079817.3:c.4098G>T
|
NP_001073285.1:p.Arg1366=
|
|