ENST00000700029.2:c.1282C>G
|
ENSP00000514759.2:p.His428Asp
|
|
ENST00000710265.1:c.*218C>G
|
ENSP00000518161.1:n.*218C>G
|
|
ENST00000688158.2:n.1924C>G
|
|
|
ENST00000688922.2:c.*1019C>G
|
ENSP00000508742.2:n.*1019C>G
|
|
ENST00000700021.1:c.1144C>G
|
ENSP00000514757.1:p.His382Asp
|
|
ENST00000700022.1:c.*528C>G
|
ENSP00000514758.1:n.*528C>G
|
|
ENST00000700023.1:n.2347C>G
|
|
|
ENST00000700024.1:n.2581C>G
|
|
|
ENST00000706954.1:c.1189C>G
|
ENSP00000516674.1:p.His397Asp
|
|
ENST00000706955.1:c.*1224C>G
|
ENSP00000516675.1:n.*1224C>G
|
|
ENST00000686459.1:c.*775C>G
|
ENSP00000508909.1:n.*775C>G
|
|
ENST00000688158.1:c.*1300C>G
|
ENSP00000509254.1:n.*1300C>G
|
|
ENST00000688308.1:c.1189C>G
|
ENSP00000508752.1:p.His397Asp
|
|
ENST00000688922.1:c.1110C>G
|
|
|
ENST00000693560.1:c.1708C>G
|
ENSP00000509861.1:p.His570Asp
|
|
ENST00000371953.8:c.1189C>G
MANE Select
|
ENSP00000361021.3:p.His397Asp
|
|
ENST00000371953.7:c.1189C>G
|
ENSP00000361021.3:p.His397Asp
|
|
NM_000314.5:c.1189C>G
|
NP_000305.3:p.His397Asp
|
|
NM_000314.6:c.1189C>G
|
NP_000305.3:p.His397Asp
|
|
NM_001304717.2:c.1708C>G
|
NP_001291646.2:p.His570Asp
|
|
NM_001304718.1:c.598C>G
|
NP_001291647.1:p.His200Asp
|
|
XM_006717926.2:c.1144C>G
|
XP_006717989.1:p.His382Asp
|
|
XM_011539982.1:c.1093C>G
|
XP_011538284.1:p.His365Asp
|
|
XR_945791.1:n.1759C>G
|
|
|
NM_000314.7:c.1189C>G
|
NP_000305.3:p.His397Asp
|
|
NM_001304717.5:c.1708C>G
|
NP_001291646.4:p.His570Asp
|
|
NM_001304718.2:c.598C>G
|
NP_001291647.1:p.His200Asp
|
|
NM_000314.8:c.1189C>G
MANE Select
|
NP_000305.3:p.His397Asp
|
|