ENST00000302850.10:c.4122G>A
MANE Select
|
ENSP00000303830.4:p.Leu1374=
|
|
ENST00000302850.9:c.4122G>A
|
ENSP00000303830.4:p.Leu1374=
|
|
ENST00000341500.9:c.4086G>A
|
ENSP00000342838.4:p.Leu1362=
|
|
NM_000208.2:c.4122G>A
|
NP_000199.2:p.Leu1374=
|
|
NM_000208.3:c.4122G>A
|
NP_000199.2:p.Leu1374=
|
|
NM_001079817.1:c.4086G>A
|
NP_001073285.1:p.Leu1362=
|
|
NM_001079817.2:c.4086G>A
|
NP_001073285.1:p.Leu1362=
|
|
XM_011527988.1:c.4197G>A
|
XP_011526290.1:p.Leu1399=
|
|
XM_011527989.1:c.4161G>A
|
XP_011526291.1:p.Leu1387=
|
|
XM_011527988.2:c.4119G>A
|
XP_011526290.2:p.Leu1373=
|
|
XM_011527989.3:c.4083G>A
|
XP_011526291.2:p.Leu1361=
|
|
NM_000208.4:c.4122G>A
MANE Select
|
NP_000199.2:p.Leu1374=
|
|
NM_001079817.3:c.4086G>A
|
NP_001073285.1:p.Leu1362=
|
|