ENST00000700029.2:c.1217A>C
|
ENSP00000514759.2:p.Asp406Ala
|
|
ENST00000710265.1:c.*153A>C
|
ENSP00000518161.1:n.*153A>C
|
|
ENST00000688158.2:n.1859A>C
|
|
|
ENST00000688922.2:c.*954A>C
|
ENSP00000508742.2:n.*954A>C
|
|
ENST00000700021.1:c.1079A>C
|
ENSP00000514757.1:p.Asp360Ala
|
|
ENST00000700022.1:c.*463A>C
|
ENSP00000514758.1:n.*463A>C
|
|
ENST00000700023.1:n.2282A>C
|
|
|
ENST00000700024.1:n.2516A>C
|
|
|
ENST00000706954.1:c.1124A>C
|
ENSP00000516674.1:p.Asp375Ala
|
|
ENST00000706955.1:c.*1159A>C
|
ENSP00000516675.1:n.*1159A>C
|
|
ENST00000686459.1:c.*710A>C
|
ENSP00000508909.1:n.*710A>C
|
|
ENST00000688158.1:c.*1235A>C
|
ENSP00000509254.1:n.*1235A>C
|
|
ENST00000688308.1:c.1124A>C
|
ENSP00000508752.1:p.Asp375Ala
|
|
ENST00000688922.1:c.1045A>C
|
|
|
ENST00000693560.1:c.1643A>C
|
ENSP00000509861.1:p.Asp548Ala
|
|
ENST00000371953.8:c.1124A>C
MANE Select
|
ENSP00000361021.3:p.Asp375Ala
|
|
ENST00000371953.7:c.1124A>C
|
ENSP00000361021.3:p.Asp375Ala
|
|
NM_000314.5:c.1124A>C
|
NP_000305.3:p.Asp375Ala
|
|
NM_000314.6:c.1124A>C
|
NP_000305.3:p.Asp375Ala
|
|
NM_001304717.2:c.1643A>C
|
NP_001291646.2:p.Asp548Ala
|
|
NM_001304718.1:c.533A>C
|
NP_001291647.1:p.Asp178Ala
|
|
XM_006717926.2:c.1079A>C
|
XP_006717989.1:p.Asp360Ala
|
|
XM_011539982.1:c.1028A>C
|
XP_011538284.1:p.Asp343Ala
|
|
XR_945791.1:n.1694A>C
|
|
|
NM_000314.7:c.1124A>C
|
NP_000305.3:p.Asp375Ala
|
|
NM_001304717.5:c.1643A>C
|
NP_001291646.4:p.Asp548Ala
|
|
NM_001304718.2:c.533A>C
|
NP_001291647.1:p.Asp178Ala
|
|
NM_000314.8:c.1124A>C
MANE Select
|
NP_000305.3:p.Asp375Ala
|
|