ENST00000302850.10:c.3882G>C
MANE Select
|
ENSP00000303830.4:p.Leu1294=
|
|
ENST00000302850.9:c.3882G>C
|
ENSP00000303830.4:p.Leu1294=
|
|
ENST00000341500.9:c.3846G>C
|
ENSP00000342838.4:p.Leu1282=
|
|
NM_000208.2:c.3882G>C
|
NP_000199.2:p.Leu1294=
|
|
NM_000208.3:c.3882G>C
|
NP_000199.2:p.Leu1294=
|
|
NM_001079817.1:c.3846G>C
|
NP_001073285.1:p.Leu1282=
|
|
NM_001079817.2:c.3846G>C
|
NP_001073285.1:p.Leu1282=
|
|
XM_011527988.1:c.3957G>C
|
XP_011526290.1:p.Leu1319=
|
|
XM_011527989.1:c.3921G>C
|
XP_011526291.1:p.Leu1307=
|
|
XM_011527988.2:c.3879G>C
|
XP_011526290.2:p.Leu1293=
|
|
XM_011527989.3:c.3843G>C
|
XP_011526291.2:p.Leu1281=
|
|
NM_000208.4:c.3882G>C
MANE Select
|
NP_000199.2:p.Leu1294=
|
|
NM_001079817.3:c.3846G>C
|
NP_001073285.1:p.Leu1282=
|
|