ENST00000302850.10:c.4149A>G
MANE Select
|
ENSP00000303830.4:p.Ter1383=
|
|
ENST00000302850.9:c.4149A>G
|
ENSP00000303830.4:p.Ter1383=
|
|
ENST00000341500.9:c.4113A>G
|
ENSP00000342838.4:p.Ter1371=
|
|
NM_000208.2:c.4149A>G
|
NP_000199.2:p.Ter1383=
|
|
NM_000208.3:c.4149A>G
|
NP_000199.2:p.Ter1383=
|
|
NM_001079817.1:c.4113A>G
|
NP_001073285.1:p.Ter1371=
|
|
NM_001079817.2:c.4113A>G
|
NP_001073285.1:p.Ter1371=
|
|
XM_011527988.1:c.4224A>G
|
XP_011526290.1:p.Ter1408=
|
|
XM_011527989.1:c.4188A>G
|
XP_011526291.1:p.Ter1396=
|
|
XM_011527988.2:c.4146A>G
|
XP_011526290.2:p.Ter1382=
|
|
XM_011527989.3:c.4110A>G
|
XP_011526291.2:p.Ter1370=
|
|
NM_000208.4:c.4149A>G
MANE Select
|
NP_000199.2:p.Ter1383=
|
|
NM_001079817.3:c.4113A>G
|
NP_001073285.1:p.Ter1371=
|
|