ENST00000302850.10:c.3883C>T
MANE Select
|
ENSP00000303830.4:p.His1295Tyr
|
|
ENST00000302850.9:c.3883C>T
|
ENSP00000303830.4:p.His1295Tyr
|
|
ENST00000341500.9:c.3847C>T
|
ENSP00000342838.4:p.His1283Tyr
|
|
NM_000208.2:c.3883C>T
|
NP_000199.2:p.His1295Tyr
|
|
NM_000208.3:c.3883C>T
|
NP_000199.2:p.His1295Tyr
|
|
NM_001079817.1:c.3847C>T
|
NP_001073285.1:p.His1283Tyr
|
|
NM_001079817.2:c.3847C>T
|
NP_001073285.1:p.His1283Tyr
|
|
XM_011527988.1:c.3958C>T
|
XP_011526290.1:p.His1320Tyr
|
|
XM_011527989.1:c.3922C>T
|
XP_011526291.1:p.His1308Tyr
|
|
XM_011527988.2:c.3880C>T
|
XP_011526290.2:p.His1294Tyr
|
|
XM_011527989.3:c.3844C>T
|
XP_011526291.2:p.His1282Tyr
|
|
NM_000208.4:c.3883C>T
MANE Select
|
NP_000199.2:p.His1295Tyr
|
|
NM_001079817.3:c.3847C>T
|
NP_001073285.1:p.His1283Tyr
|
|