ENST00000302850.10:c.4009A>C
MANE Select
|
ENSP00000303830.4:p.Arg1337=
|
|
ENST00000302850.9:c.4009A>C
|
ENSP00000303830.4:p.Arg1337=
|
|
ENST00000341500.9:c.3973A>C
|
ENSP00000342838.4:p.Arg1325=
|
|
NM_000208.2:c.4009A>C
|
NP_000199.2:p.Arg1337=
|
|
NM_000208.3:c.4009A>C
|
NP_000199.2:p.Arg1337=
|
|
NM_001079817.1:c.3973A>C
|
NP_001073285.1:p.Arg1325=
|
|
NM_001079817.2:c.3973A>C
|
NP_001073285.1:p.Arg1325=
|
|
XM_011527988.1:c.4084A>C
|
XP_011526290.1:p.Arg1362=
|
|
XM_011527989.1:c.4048A>C
|
XP_011526291.1:p.Arg1350=
|
|
XM_011527988.2:c.4006A>C
|
XP_011526290.2:p.Arg1336=
|
|
XM_011527989.3:c.3970A>C
|
XP_011526291.2:p.Arg1324=
|
|
NM_000208.4:c.4009A>C
MANE Select
|
NP_000199.2:p.Arg1337=
|
|
NM_001079817.3:c.3973A>C
|
NP_001073285.1:p.Arg1325=
|
|