ENST00000695651.1:n.2030T>C
|
|
|
ENST00000695652.1:c.3559T>C
|
ENSP00000512083.1:p.Tyr1187His
|
|
ENST00000695653.1:c.1591T>C
|
ENSP00000512084.1:p.Tyr531His
|
|
ENST00000695654.1:c.2707T>C
|
ENSP00000512085.1:p.Tyr903His
|
|
ENST00000695655.1:c.2623T>C
|
ENSP00000512086.1:n.2623T>C
|
|
ENST00000695692.1:n.3046T>C
|
|
|
ENST00000245907.11:c.3682T>C
MANE Select
|
ENSP00000245907.4:p.Tyr1228His
|
|
ENST00000245907.10:c.3682T>C
|
ENSP00000245907.4:p.Tyr1228His
|
|
ENST00000596238.1:n.125T>C
|
|
|
ENST00000601008.1:c.241+494T>C
|
ENSP00000471384.1:n.241+494T>C
|
|
NM_000064.3:c.3682T>C
|
NP_000055.2:p.Tyr1228His
|
|
NM_000064.4:c.3682T>C
MANE Select
|
NP_000055.2:p.Tyr1228His
|
|