ENST00000302850.10:c.3023G=
MANE Select
|
ENSP00000303830.4:p.Cys1008=
|
|
ENST00000302850.9:c.3023G=
|
ENSP00000303830.4:p.Cys1008=
|
|
ENST00000341500.9:c.2987G=
|
ENSP00000342838.4:p.Cys996=
|
|
NM_000208.2:c.3023G=
|
NP_000199.2:p.Cys1008=
|
|
NM_000208.3:c.3023G=
|
NP_000199.2:p.Cys1008=
|
|
NM_001079817.1:c.2987G=
|
NP_001073285.1:p.Cys996=
|
|
NM_001079817.2:c.2987G=
|
NP_001073285.1:p.Cys996=
|
|
XM_011527988.1:c.3098G=
|
XP_011526290.1:p.Cys1033=
|
|
XM_011527989.1:c.3062G=
|
XP_011526291.1:p.Cys1021=
|
|
XM_011527988.2:c.3020G=
|
XP_011526290.2:p.Cys1007=
|
|
XM_011527989.3:c.2984G=
|
XP_011526291.2:p.Cys995=
|
|
NM_000208.4:c.3023G=
MANE Select
|
NP_000199.2:p.Cys1008=
|
|
NM_001079817.3:c.2987G=
|
NP_001073285.1:p.Cys996=
|
|