ENST00000695651.1:n.2034A>T
|
|
|
ENST00000695652.1:c.3563A>T
|
ENSP00000512083.1:p.Asn1188Ile
|
|
ENST00000695653.1:c.1595A>T
|
ENSP00000512084.1:p.Asn532Ile
|
|
ENST00000695654.1:c.2711A>T
|
ENSP00000512085.1:p.Asn904Ile
|
|
ENST00000695655.1:c.2627A>T
|
ENSP00000512086.1:n.2627A>T
|
|
ENST00000695692.1:n.3050A>T
|
|
|
ENST00000245907.11:c.3686A>T
MANE Select
|
ENSP00000245907.4:p.Asn1229Ile
|
|
ENST00000245907.10:c.3686A>T
|
ENSP00000245907.4:p.Asn1229Ile
|
|
ENST00000596238.1:n.129A>T
|
|
|
ENST00000601008.1:c.241+498A>T
|
ENSP00000471384.1:n.241+498A>T
|
|
NM_000064.3:c.3686A>T
|
NP_000055.2:p.Asn1229Ile
|
|
NM_000064.4:c.3686A>T
MANE Select
|
NP_000055.2:p.Asn1229Ile
|
|