ENST00000695651.1:n.1103C>T
|
|
|
ENST00000695652.1:c.2632C>T
|
ENSP00000512083.1:p.His878Tyr
|
|
ENST00000695653.1:c.664C>T
|
ENSP00000512084.1:p.His222Tyr
|
|
ENST00000695654.1:c.1879C>T
|
ENSP00000512085.1:p.His627Tyr
|
|
ENST00000695655.1:c.1696C>T
|
ENSP00000512086.1:n.1696C>T
|
|
ENST00000695692.1:n.2119C>T
|
|
|
ENST00000245907.11:c.2755C>T
MANE Select
|
ENSP00000245907.4:p.His919Tyr
|
|
ENST00000245907.10:c.2755C>T
|
ENSP00000245907.4:p.His919Tyr
|
|
ENST00000594005.1:n.331C>T
|
|
|
NM_000064.3:c.2755C>T
|
NP_000055.2:p.His919Tyr
|
|
NM_000064.4:c.2755C>T
MANE Select
|
NP_000055.2:p.His919Tyr
|
|