ENST00000695651.1:n.2033A>C
|
|
|
ENST00000695652.1:c.3562A>C
|
ENSP00000512083.1:p.Asn1188His
|
|
ENST00000695653.1:c.1594A>C
|
ENSP00000512084.1:p.Asn532His
|
|
ENST00000695654.1:c.2710A>C
|
ENSP00000512085.1:p.Asn904His
|
|
ENST00000695655.1:c.2626A>C
|
ENSP00000512086.1:n.2626A>C
|
|
ENST00000695692.1:n.3049A>C
|
|
|
ENST00000245907.11:c.3685A>C
MANE Select
|
ENSP00000245907.4:p.Asn1229His
|
|
ENST00000245907.10:c.3685A>C
|
ENSP00000245907.4:p.Asn1229His
|
|
ENST00000596238.1:n.128A>C
|
|
|
ENST00000601008.1:c.241+497A>C
|
ENSP00000471384.1:n.241+497A>C
|
|
NM_000064.3:c.3685A>C
|
NP_000055.2:p.Asn1229His
|
|
NM_000064.4:c.3685A>C
MANE Select
|
NP_000055.2:p.Asn1229His
|
|