ENST00000700029.2:c.980_983delinsGTGA
|
ENSP00000514759.2:p.Cys327=
|
|
ENST00000710265.1:c.887_890delinsGTGA
|
ENSP00000518161.1:p.Cys296=
|
|
ENST00000472832.3:c.887_890delinsGTGA
|
ENSP00000483066.2:p.Cys296=
|
|
ENST00000688158.2:n.1622_1625delinsGTGA
|
|
|
ENST00000688922.2:c.*717_*720delinsGTGA
|
ENSP00000508742.2:n.*717_*720delinsGTGA
|
|
ENST00000700021.1:c.842_845delinsGTGA
|
ENSP00000514757.1:p.Cys281=
|
|
ENST00000700022.1:c.*226_*229delinsGTGA
|
ENSP00000514758.1:n.*226_*229delinsGTGA
|
|
ENST00000700023.1:n.2045_2048delinsGTGA
|
|
|
ENST00000700024.1:n.2279_2282delinsGTGA
|
|
|
ENST00000700025.1:n.1656_1659delinsGTGA
|
|
|
ENST00000700026.1:n.524_527delinsGTGA
|
|
|
ENST00000706954.1:c.887_890delinsGTGA
|
ENSP00000516674.1:p.Cys296=
|
|
ENST00000706955.1:c.*922_*925delinsGTGA
|
ENSP00000516675.1:n.*922_*925delinsGTGA
|
|
ENST00000686459.1:c.*473_*476delinsGTGA
|
ENSP00000508909.1:n.*473_*476delinsGTGA
|
|
ENST00000688158.1:c.*998_*1001delinsGTGA
|
ENSP00000509254.1:n.*998_*1001delinsGTGA
|
|
ENST00000688308.1:c.887_890delinsGTGA
|
ENSP00000508752.1:p.Cys296=
|
|
ENST00000688922.1:c.808_811delinsGTGA
|
|
|
ENST00000693560.1:c.1406_1409delinsGTGA
|
ENSP00000509861.1:p.Cys469=
|
|
ENST00000371953.8:c.887_890delinsGTGA
MANE Select
|
ENSP00000361021.3:p.Cys296=
|
|
ENST00000371953.7:c.887_890delinsGTGA
|
ENSP00000361021.3:p.Cys296=
|
|
ENST00000472832.2:c.314_317delinsGTGA
|
ENSP00000483066.1:p.Cys105=
|
|
NM_000314.5:c.887_890delinsGTGA
|
NP_000305.3:p.Cys296=
|
|
NM_000314.6:c.887_890delinsGTGA
|
NP_000305.3:p.Cys296=
|
|
NM_001304717.2:c.1406_1409delinsGTGA
|
NP_001291646.2:p.Cys469=
|
|
NM_001304718.1:c.296_299delinsGTGA
|
NP_001291647.1:p.Cys99=
|
|
XM_006717926.2:c.842_845delinsGTGA
|
XP_006717989.1:p.Cys281=
|
|
XM_011539981.1:c.887_890delinsGTGA
|
XP_011538283.1:p.Cys296=
|
|
XM_011539982.1:c.791_794delinsGTGA
|
XP_011538284.1:p.Cys264=
|
|
XR_945791.1:n.1457_1460delinsGTGA
|
|
|
NM_000314.7:c.887_890delinsGTGA
|
NP_000305.3:p.Cys296=
|
|
NM_001304717.5:c.1406_1409delinsGTGA
|
NP_001291646.4:p.Cys469=
|
|
NM_001304718.2:c.296_299delinsGTGA
|
NP_001291647.1:p.Cys99=
|
|
NM_000314.8:c.887_890delinsGTGA
MANE Select
|
NP_000305.3:p.Cys296=
|
|