ENST00000695651.1:n.992C>T
|
|
|
ENST00000695652.1:c.2521C>T
|
ENSP00000512083.1:p.His841Tyr
|
|
ENST00000695653.1:c.553C>T
|
ENSP00000512084.1:p.His185Tyr
|
|
ENST00000695654.1:c.1768C>T
|
ENSP00000512085.1:p.His590Tyr
|
|
ENST00000695655.1:c.1585C>T
|
ENSP00000512086.1:n.1585C>T
|
|
ENST00000695692.1:n.2008C>T
|
|
|
ENST00000245907.11:c.2644C>T
MANE Select
|
ENSP00000245907.4:p.His882Tyr
|
|
ENST00000245907.10:c.2644C>T
|
ENSP00000245907.4:p.His882Tyr
|
|
ENST00000594005.1:n.220C>T
|
|
|
NM_000064.3:c.2644C>T
|
NP_000055.2:p.His882Tyr
|
|
NM_000064.4:c.2644C>T
MANE Select
|
NP_000055.2:p.His882Tyr
|
|