|
ENST00000700029.2:c.634+1G>C
|
ENSP00000514759.2:n.634+1G>C
|
|
|
ENST00000710265.1:c.634+1G>C
|
ENSP00000518161.1:n.634+1G>C
|
|
|
ENST00000472832.3:c.634+1G>C
|
ENSP00000483066.2:n.634+1G>C
|
|
|
ENST00000688158.2:n.1369+1G>C
|
|
|
|
ENST00000688922.2:c.*464+1G>C
|
ENSP00000508742.2:n.*464+1G>C
|
|
|
ENST00000700021.1:c.589+1G>C
|
ENSP00000514757.1:n.589+1G>C
|
|
|
ENST00000700022.1:c.493-5593G>C
|
ENSP00000514758.1:n.493-5593G>C
|
|
|
ENST00000700023.1:n.1792+1G>C
|
|
|
|
ENST00000700024.1:n.2026+1G>C
|
|
|
|
ENST00000700025.1:n.1403+1G>C
|
|
|
|
ENST00000700029.1:c.468+1G>C
|
|
|
|
ENST00000706954.1:c.634+1G>C
|
ENSP00000516674.1:n.634+1G>C
|
|
|
ENST00000706955.1:c.*669+1G>C
|
ENSP00000516675.1:n.*669+1G>C
|
|
|
ENST00000686459.1:c.*220+1G>C
|
ENSP00000508909.1:n.*220+1G>C
|
|
|
ENST00000688158.1:c.*745+1G>C
|
ENSP00000509254.1:n.*745+1G>C
|
|
|
ENST00000688308.1:c.634+1G>C
|
ENSP00000508752.1:n.634+1G>C
|
|
|
ENST00000688922.1:c.555+1G>C
|
|
|
|
ENST00000693560.1:c.1153+1G>C
|
ENSP00000509861.1:n.1153+1G>C
|
|
|
ENST00000371953.8:c.634+1G>C
MANE Select
|
ENSP00000361021.3:n.634+1G>C
|
|
|
ENST00000371953.7:c.634+1G>C
|
ENSP00000361021.3:n.634+1G>C
|
|
|
ENST00000472832.2:c.61+1G>C
|
ENSP00000483066.1:n.61+1G>C
|
|
|
NM_000314.5:c.634+1G>C
|
NP_000305.3:n.634+1G>C
|
|
|
NM_000314.6:c.634+1G>C
|
NP_000305.3:n.634+1G>C
|
|
|
NM_001304717.2:c.1153+1G>C
|
NP_001291646.2:n.1153+1G>C
|
|
|
NM_001304718.1:c.43+1G>C
|
NP_001291647.1:n.43+1G>C
|
|
|
XM_006717926.2:c.589+1G>C
|
XP_006717989.1:n.589+1G>C
|
|
|
XM_011539981.1:c.634+1G>C
|
XP_011538283.1:n.634+1G>C
|
|
|
XM_011539982.1:c.538+1G>C
|
XP_011538284.1:n.538+1G>C
|
|
|
XR_945791.1:n.1205-5593G>C
|
|
|
|
NM_000314.7:c.634+1G>C
|
NP_000305.3:n.634+1G>C
|
|
|
NM_001304717.5:c.1153+1G>C
|
NP_001291646.4:n.1153+1G>C
|
|
|
NM_001304718.2:c.43+1G>C
|
NP_001291647.1:n.43+1G>C
|
|
|
NM_000314.8:c.634+1G>C
MANE Select
|
NP_000305.3:n.634+1G>C
|
|
