ENST00000695651.1:n.908T>C
|
|
|
ENST00000695652.1:c.2437T>C
|
ENSP00000512083.1:p.Tyr813His
|
|
ENST00000695653.1:c.469T>C
|
ENSP00000512084.1:p.Tyr157His
|
|
ENST00000695654.1:c.1684T>C
|
ENSP00000512085.1:p.Tyr562His
|
|
ENST00000695655.1:c.1501T>C
|
ENSP00000512086.1:n.1501T>C
|
|
ENST00000695692.1:n.1924T>C
|
|
|
ENST00000245907.11:c.2560T>C
MANE Select
|
ENSP00000245907.4:p.Tyr854His
|
|
ENST00000245907.10:c.2560T>C
|
ENSP00000245907.4:p.Tyr854His
|
|
ENST00000594005.1:n.41T>C
|
|
|
ENST00000602053.1:n.608T>C
|
|
|
NM_000064.3:c.2560T>C
|
NP_000055.2:p.Tyr854His
|
|
NM_000064.4:c.2560T>C
MANE Select
|
NP_000055.2:p.Tyr854His
|
|