|
ENST00000700029.2:c.784_786delinsGAT
|
ENSP00000514759.2:p.Asn262Asp
|
|
|
ENST00000710265.1:c.784_786delinsGAT
|
ENSP00000518161.1:p.Asn262Asp
|
|
|
ENST00000472832.3:c.784_786delinsGAT
|
ENSP00000483066.2:p.Asn262Asp
|
|
|
ENST00000688158.2:n.1519_1521delinsGAT
|
|
|
|
ENST00000688922.2:c.*614_*616delinsGAT
|
ENSP00000508742.2:n.*614_*616delinsGAT
|
|
|
ENST00000700021.1:c.739_741delinsGAT
|
ENSP00000514757.1:p.Asn247Asp
|
|
|
ENST00000700022.1:c.*123_*125delinsGAT
|
ENSP00000514758.1:n.*123_*125delinsGAT
|
|
|
ENST00000700023.1:n.1942_1944delinsGAT
|
|
|
|
ENST00000700024.1:n.2176_2178delinsGAT
|
|
|
|
ENST00000700025.1:n.1553_1555delinsGAT
|
|
|
|
ENST00000700026.1:n.421_423delinsGAT
|
|
|
|
ENST00000700029.1:c.618_620delinsGAT
|
|
|
|
ENST00000706954.1:c.784_786delinsGAT
|
ENSP00000516674.1:p.Asn262Asp
|
|
|
ENST00000706955.1:c.*819_*821delinsGAT
|
ENSP00000516675.1:n.*819_*821delinsGAT
|
|
|
ENST00000686459.1:c.*370_*372delinsGAT
|
ENSP00000508909.1:n.*370_*372delinsGAT
|
|
|
ENST00000688158.1:c.*895_*897delinsGAT
|
ENSP00000509254.1:n.*895_*897delinsGAT
|
|
|
ENST00000688308.1:c.784_786delinsGAT
|
ENSP00000508752.1:p.Asn262Asp
|
|
|
ENST00000688922.1:c.705_707delinsGAT
|
|
|
|
ENST00000693560.1:c.1303_1305delinsGAT
|
ENSP00000509861.1:p.Asn435Asp
|
|
|
ENST00000371953.8:c.784_786delinsGAT
MANE Select
|
ENSP00000361021.3:p.Asn262Asp
|
|
|
ENST00000371953.7:c.784_786delinsGAT
|
ENSP00000361021.3:p.Asn262Asp
|
|
|
ENST00000472832.2:c.211_213delinsGAT
|
ENSP00000483066.1:p.Asn71Asp
|
|
|
NM_000314.5:c.784_786delinsGAT
|
NP_000305.3:p.Asn262Asp
|
|
|
NM_000314.6:c.784_786delinsGAT
|
NP_000305.3:p.Asn262Asp
|
|
|
NM_001304717.2:c.1303_1305delinsGAT
|
NP_001291646.2:p.Asn435Asp
|
|
|
NM_001304718.1:c.193_195delinsGAT
|
NP_001291647.1:p.Asn65Asp
|
|
|
XM_006717926.2:c.739_741delinsGAT
|
XP_006717989.1:p.Asn247Asp
|
|
|
XM_011539981.1:c.784_786delinsGAT
|
XP_011538283.1:p.Asn262Asp
|
|
|
XM_011539982.1:c.688_690delinsGAT
|
XP_011538284.1:p.Asn230Asp
|
|
|
XR_945791.1:n.1354_1356delinsGAT
|
|
|
|
NM_000314.7:c.784_786delinsGAT
|
NP_000305.3:p.Asn262Asp
|
|
|
NM_001304717.5:c.1303_1305delinsGAT
|
NP_001291646.4:p.Asn435Asp
|
|
|
NM_001304718.2:c.193_195delinsGAT
|
NP_001291647.1:p.Asn65Asp
|
|
|
NM_000314.8:c.784_786delinsGAT
MANE Select
|
NP_000305.3:p.Asn262Asp
|
|
