ENST00000700029.2:c.1079A>T
|
ENSP00000514759.2:p.Asn360Ile
|
|
ENST00000710265.1:c.986A>T
|
ENSP00000518161.1:p.Asn329Ile
|
|
ENST00000472832.3:c.986A>T
|
ENSP00000483066.2:p.Asn329Ile
|
|
ENST00000688158.2:n.1721A>T
|
|
|
ENST00000688922.2:c.*816A>T
|
ENSP00000508742.2:n.*816A>T
|
|
ENST00000700021.1:c.941A>T
|
ENSP00000514757.1:p.Asn314Ile
|
|
ENST00000700022.1:c.*325A>T
|
ENSP00000514758.1:n.*325A>T
|
|
ENST00000700023.1:n.2144A>T
|
|
|
ENST00000700024.1:n.2378A>T
|
|
|
ENST00000700025.1:n.1755A>T
|
|
|
ENST00000700026.1:n.623A>T
|
|
|
ENST00000706954.1:c.986A>T
|
ENSP00000516674.1:p.Asn329Ile
|
|
ENST00000706955.1:c.*1021A>T
|
ENSP00000516675.1:n.*1021A>T
|
|
ENST00000686459.1:c.*572A>T
|
ENSP00000508909.1:n.*572A>T
|
|
ENST00000688158.1:c.*1097A>T
|
ENSP00000509254.1:n.*1097A>T
|
|
ENST00000688308.1:c.986A>T
|
ENSP00000508752.1:p.Asn329Ile
|
|
ENST00000688922.1:c.907A>T
|
|
|
ENST00000693560.1:c.1505A>T
|
ENSP00000509861.1:p.Asn502Ile
|
|
ENST00000371953.8:c.986A>T
MANE Select
|
ENSP00000361021.3:p.Asn329Ile
|
|
ENST00000371953.7:c.986A>T
|
ENSP00000361021.3:p.Asn329Ile
|
|
ENST00000472832.2:c.413A>T
|
ENSP00000483066.1:p.Asn138Ile
|
|
NM_000314.5:c.986A>T
|
NP_000305.3:p.Asn329Ile
|
|
NM_000314.6:c.986A>T
|
NP_000305.3:p.Asn329Ile
|
|
NM_001304717.2:c.1505A>T
|
NP_001291646.2:p.Asn502Ile
|
|
NM_001304718.1:c.395A>T
|
NP_001291647.1:p.Asn132Ile
|
|
XM_006717926.2:c.941A>T
|
XP_006717989.1:p.Asn314Ile
|
|
XM_011539981.1:c.986A>T
|
XP_011538283.1:p.Asn329Ile
|
|
XM_011539982.1:c.890A>T
|
XP_011538284.1:p.Asn297Ile
|
|
XR_945791.1:n.1556A>T
|
|
|
NM_000314.7:c.986A>T
|
NP_000305.3:p.Asn329Ile
|
|
NM_001304717.5:c.1505A>T
|
NP_001291646.4:p.Asn502Ile
|
|
NM_001304718.2:c.395A>T
|
NP_001291647.1:p.Asn132Ile
|
|
NM_000314.8:c.986A>T
MANE Select
|
NP_000305.3:p.Asn329Ile
|
|