ENST00000695651.1:n.2000A>C
|
|
|
ENST00000695652.1:c.3529A>C
|
ENSP00000512083.1:p.Asn1177His
|
|
ENST00000695653.1:c.1561A>C
|
ENSP00000512084.1:p.Asn521His
|
|
ENST00000695654.1:c.2677A>C
|
ENSP00000512085.1:p.Asn893His
|
|
ENST00000695655.1:c.2593A>C
|
ENSP00000512086.1:n.2593A>C
|
|
ENST00000695692.1:n.3016A>C
|
|
|
ENST00000245907.11:c.3652A>C
MANE Select
|
ENSP00000245907.4:p.Asn1218His
|
|
ENST00000245907.10:c.3652A>C
|
ENSP00000245907.4:p.Asn1218His
|
|
ENST00000596238.1:n.95A>C
|
|
|
ENST00000601008.1:c.241+464A>C
|
ENSP00000471384.1:n.241+464A>C
|
|
NM_000064.3:c.3652A>C
|
NP_000055.2:p.Asn1218His
|
|
NM_000064.4:c.3652A>C
MANE Select
|
NP_000055.2:p.Asn1218His
|
|