|
ENST00000700029.2:c.1120-135A>C
|
ENSP00000514759.2:n.1120-135A>C
|
|
|
ENST00000710265.1:c.*56-135A>C
|
ENSP00000518161.1:n.*56-135A>C
|
|
|
ENST00000688158.2:n.1762-135A>C
|
|
|
|
ENST00000688922.2:c.*857-135A>C
|
ENSP00000508742.2:n.*857-135A>C
|
|
|
ENST00000700021.1:c.982-135A>C
|
ENSP00000514757.1:n.982-135A>C
|
|
|
ENST00000700022.1:c.*366-135A>C
|
ENSP00000514758.1:n.*366-135A>C
|
|
|
ENST00000700023.1:n.2185-135A>C
|
|
|
|
ENST00000700024.1:n.2419-135A>C
|
|
|
|
ENST00000706954.1:c.1027-135A>C
|
ENSP00000516674.1:n.1027-135A>C
|
|
|
ENST00000706955.1:c.*1062-135A>C
|
ENSP00000516675.1:n.*1062-135A>C
|
|
|
ENST00000686459.1:c.*613-135A>C
|
ENSP00000508909.1:n.*613-135A>C
|
|
|
ENST00000688158.1:c.*1138-135A>C
|
ENSP00000509254.1:n.*1138-135A>C
|
|
|
ENST00000688308.1:c.1027-135A>C
|
ENSP00000508752.1:n.1027-135A>C
|
|
|
ENST00000688922.1:c.948-135A>C
|
|
|
|
ENST00000693560.1:c.1546-135A>C
|
ENSP00000509861.1:n.1546-135A>C
|
|
|
ENST00000371953.8:c.1027-135A>C
MANE Select
|
ENSP00000361021.3:n.1027-135A>C
|
|
|
ENST00000371953.7:c.1027-135A>C
|
ENSP00000361021.3:n.1027-135A>C
|
|
|
NM_000314.5:c.1027-135A>C
|
NP_000305.3:n.1027-135A>C
|
|
|
NM_000314.6:c.1027-135A>C
|
NP_000305.3:n.1027-135A>C
|
|
|
NM_001304717.2:c.1546-135A>C
|
NP_001291646.2:n.1546-135A>C
|
|
|
NM_001304718.1:c.436-135A>C
|
NP_001291647.1:n.436-135A>C
|
|
|
XM_006717926.2:c.982-135A>C
|
XP_006717989.1:n.982-135A>C
|
|
|
XM_011539982.1:c.931-135A>C
|
XP_011538284.1:n.931-135A>C
|
|
|
XR_945791.1:n.1597-135A>C
|
|
|
|
NM_000314.7:c.1027-135A>C
|
NP_000305.3:n.1027-135A>C
|
|
|
NM_001304717.5:c.1546-135A>C
|
NP_001291646.4:n.1546-135A>C
|
|
|
NM_001304718.2:c.436-135A>C
|
NP_001291647.1:n.436-135A>C
|
|
|
NM_000314.8:c.1027-135A>C
MANE Select
|
NP_000305.3:n.1027-135A>C
|
|
