ENST00000302850.10:c.4145C>A
MANE Select
|
ENSP00000303830.4:p.Ser1382Tyr
|
|
ENST00000302850.9:c.4145C>A
|
ENSP00000303830.4:p.Ser1382Tyr
|
|
ENST00000341500.9:c.4109C>A
|
ENSP00000342838.4:p.Ser1370Tyr
|
|
NM_000208.2:c.4145C>A
|
NP_000199.2:p.Ser1382Tyr
|
|
NM_000208.3:c.4145C>A
|
NP_000199.2:p.Ser1382Tyr
|
|
NM_001079817.1:c.4109C>A
|
NP_001073285.1:p.Ser1370Tyr
|
|
NM_001079817.2:c.4109C>A
|
NP_001073285.1:p.Ser1370Tyr
|
|
XM_011527988.1:c.4220C>A
|
XP_011526290.1:p.Ser1407Tyr
|
|
XM_011527989.1:c.4184C>A
|
XP_011526291.1:p.Ser1395Tyr
|
|
XM_011527988.2:c.4142C>A
|
XP_011526290.2:p.Ser1381Tyr
|
|
XM_011527989.3:c.4106C>A
|
XP_011526291.2:p.Ser1369Tyr
|
|
NM_000208.4:c.4145C>A
MANE Select
|
NP_000199.2:p.Ser1382Tyr
|
|
NM_001079817.3:c.4109C>A
|
NP_001073285.1:p.Ser1370Tyr
|
|