ENST00000508233.6:c.451C>T
|
ENSP00000422973.2:p.His151Tyr
|
|
ENST00000614857.5:c.574C>T
|
ENSP00000477824.2:p.His192Tyr
|
|
ENST00000681973.1:n.801C>T
|
|
|
ENST00000682026.1:n.527C>T
|
|
|
ENST00000682448.1:n.2060C>T
|
|
|
ENST00000682554.1:n.2022C>T
|
|
|
ENST00000682599.1:n.3062C>T
|
|
|
ENST00000682627.1:n.494C>T
|
|
|
ENST00000682865.1:n.858C>T
|
|
|
ENST00000683087.1:n.588C>T
|
|
|
ENST00000683168.1:n.1328C>T
|
|
|
ENST00000683620.1:n.1756C>T
|
|
|
ENST00000684106.1:n.2824C>T
|
|
|
ENST00000684450.1:n.1633C>T
|
|
|
ENST00000684710.1:n.1865C>T
|
|
|
ENST00000395080.8:c.574C>T
MANE Select
|
ENSP00000378517.3:p.His192Tyr
|
|
ENST00000237623.11:c.532C>T
|
ENSP00000237623.7:p.His178Tyr
|
|
ENST00000360804.4:c.493C>T
|
ENSP00000354042.4:p.His165Tyr
|
|
ENST00000395080.7:c.574C>T
|
ENSP00000378517.3:p.His192Tyr
|
|
ENST00000508233.5:c.451C>T
|
ENSP00000422973.1:p.His151Tyr
|
|
ENST00000509659.5:n.863C>T
|
|
|
ENST00000614857.4:c.508C>T
|
ENSP00000477824.1:p.His170Tyr
|
|
NM_000582.2:c.532C>T
|
NP_000573.1:p.His178Tyr
|
|
NM_001040058.1:c.574C>T
|
NP_001035147.1:p.His192Tyr
|
|
NM_001040060.1:c.493C>T
|
NP_001035149.1:p.His165Tyr
|
|
NM_001251829.1:c.451C>T
|
NP_001238758.1:p.His151Tyr
|
|
NM_001251830.1:c.613C>T
|
NP_001238759.1:p.His205Tyr
|
|
NM_001040058.2:c.574C>T
MANE Select
|
NP_001035147.1:p.His192Tyr
|
|
NM_000582.3:c.532C>T
|
NP_000573.1:p.His178Tyr
|
|
NM_001040060.2:c.493C>T
|
NP_001035149.1:p.His165Tyr
|
|
NM_001251829.2:c.451C>T
|
NP_001238758.1:p.His151Tyr
|
|
NM_001251830.2:c.613C>T
|
NP_001238759.1:p.His205Tyr
|
|