|
ENST00000700029.2:c.998G>T
|
ENSP00000514759.2:p.Ser333Ile
|
|
|
ENST00000710265.1:c.905G>T
|
ENSP00000518161.1:p.Ser302Ile
|
|
|
ENST00000472832.3:c.905G>T
|
ENSP00000483066.2:p.Ser302Ile
|
|
|
ENST00000688158.2:n.1640G>T
|
|
|
|
ENST00000688922.2:c.*735G>T
|
ENSP00000508742.2:n.*735G>T
|
|
|
ENST00000700021.1:c.860G>T
|
ENSP00000514757.1:p.Ser287Ile
|
|
|
ENST00000700022.1:c.*244G>T
|
ENSP00000514758.1:n.*244G>T
|
|
|
ENST00000700023.1:n.2063G>T
|
|
|
|
ENST00000700024.1:n.2297G>T
|
|
|
|
ENST00000700025.1:n.1674G>T
|
|
|
|
ENST00000700026.1:n.542G>T
|
|
|
|
ENST00000706954.1:c.905G>T
|
ENSP00000516674.1:p.Ser302Ile
|
|
|
ENST00000706955.1:c.*940G>T
|
ENSP00000516675.1:n.*940G>T
|
|
|
ENST00000686459.1:c.*491G>T
|
ENSP00000508909.1:n.*491G>T
|
|
|
ENST00000688158.1:c.*1016G>T
|
ENSP00000509254.1:n.*1016G>T
|
|
|
ENST00000688308.1:c.905G>T
|
ENSP00000508752.1:p.Ser302Ile
|
|
|
ENST00000688922.1:c.826G>T
|
|
|
|
ENST00000693560.1:c.1424G>T
|
ENSP00000509861.1:p.Ser475Ile
|
|
|
ENST00000371953.8:c.905G>T
MANE Select
|
ENSP00000361021.3:p.Ser302Ile
|
|
|
ENST00000371953.7:c.905G>T
|
ENSP00000361021.3:p.Ser302Ile
|
|
|
ENST00000472832.2:c.332G>T
|
ENSP00000483066.1:p.Ser111Ile
|
|
|
NM_000314.5:c.905G>T
|
NP_000305.3:p.Ser302Ile
|
|
|
NM_000314.6:c.905G>T
|
NP_000305.3:p.Ser302Ile
|
|
|
NM_001304717.2:c.1424G>T
|
NP_001291646.2:p.Ser475Ile
|
|
|
NM_001304718.1:c.314G>T
|
NP_001291647.1:p.Ser105Ile
|
|
|
XM_006717926.2:c.860G>T
|
XP_006717989.1:p.Ser287Ile
|
|
|
XM_011539981.1:c.905G>T
|
XP_011538283.1:p.Ser302Ile
|
|
|
XM_011539982.1:c.809G>T
|
XP_011538284.1:p.Ser270Ile
|
|
|
XR_945791.1:n.1475G>T
|
|
|
|
NM_000314.7:c.905G>T
|
NP_000305.3:p.Ser302Ile
|
|
|
NM_001304717.5:c.1424G>T
|
NP_001291646.4:p.Ser475Ile
|
|
|
NM_001304718.2:c.314G>T
|
NP_001291647.1:p.Ser105Ile
|
|
|
NM_000314.8:c.905G>T
MANE Select
|
NP_000305.3:p.Ser302Ile
|
|
