ENST00000302850.10:c.3098C>A
MANE Select
|
ENSP00000303830.4:p.Ser1033Tyr
|
|
ENST00000302850.9:c.3098C>A
|
ENSP00000303830.4:p.Ser1033Tyr
|
|
ENST00000341500.9:c.3062C>A
|
ENSP00000342838.4:p.Ser1021Tyr
|
|
NM_000208.2:c.3098C>A
|
NP_000199.2:p.Ser1033Tyr
|
|
NM_000208.3:c.3098C>A
|
NP_000199.2:p.Ser1033Tyr
|
|
NM_001079817.1:c.3062C>A
|
NP_001073285.1:p.Ser1021Tyr
|
|
NM_001079817.2:c.3062C>A
|
NP_001073285.1:p.Ser1021Tyr
|
|
XM_011527988.1:c.3173C>A
|
XP_011526290.1:p.Ser1058Tyr
|
|
XM_011527989.1:c.3137C>A
|
XP_011526291.1:p.Ser1046Tyr
|
|
XM_011527988.2:c.3095C>A
|
XP_011526290.2:p.Ser1032Tyr
|
|
XM_011527989.3:c.3059C>A
|
XP_011526291.2:p.Ser1020Tyr
|
|
NM_000208.4:c.3098C>A
MANE Select
|
NP_000199.2:p.Ser1033Tyr
|
|
NM_001079817.3:c.3062C>A
|
NP_001073285.1:p.Ser1021Tyr
|
|