ENST00000302850.10:c.3913C>T
MANE Select
|
ENSP00000303830.4:p.His1305Tyr
|
|
ENST00000302850.9:c.3913C>T
|
ENSP00000303830.4:p.His1305Tyr
|
|
ENST00000341500.9:c.3877C>T
|
ENSP00000342838.4:p.His1293Tyr
|
|
NM_000208.2:c.3913C>T
|
NP_000199.2:p.His1305Tyr
|
|
NM_000208.3:c.3913C>T
|
NP_000199.2:p.His1305Tyr
|
|
NM_001079817.1:c.3877C>T
|
NP_001073285.1:p.His1293Tyr
|
|
NM_001079817.2:c.3877C>T
|
NP_001073285.1:p.His1293Tyr
|
|
XM_011527988.1:c.3988C>T
|
XP_011526290.1:p.His1330Tyr
|
|
XM_011527989.1:c.3952C>T
|
XP_011526291.1:p.His1318Tyr
|
|
XM_011527988.2:c.3910C>T
|
XP_011526290.2:p.His1304Tyr
|
|
XM_011527989.3:c.3874C>T
|
XP_011526291.2:p.His1292Tyr
|
|
NM_000208.4:c.3913C>T
MANE Select
|
NP_000199.2:p.His1305Tyr
|
|
NM_001079817.3:c.3877C>T
|
NP_001073285.1:p.His1293Tyr
|
|