|
ENST00000700029.2:c.1237_1239delinsGCT
|
ENSP00000514759.2:p.Thr413Ala
|
|
|
ENST00000710265.1:c.*173_*175delinsGCT
|
ENSP00000518161.1:n.*173_*175delinsGCT
|
|
|
ENST00000688158.2:n.1879_1881delinsGCT
|
|
|
|
ENST00000688922.2:c.*974_*976delinsGCT
|
ENSP00000508742.2:n.*974_*976delinsGCT
|
|
|
ENST00000700021.1:c.1099_1101delinsGCT
|
ENSP00000514757.1:p.Thr367Ala
|
|
|
ENST00000700022.1:c.*483_*485delinsGCT
|
ENSP00000514758.1:n.*483_*485delinsGCT
|
|
|
ENST00000700023.1:n.2302_2304delinsGCT
|
|
|
|
ENST00000700024.1:n.2536_2538delinsGCT
|
|
|
|
ENST00000706954.1:c.1144_1146delinsGCT
|
ENSP00000516674.1:p.Thr382Ala
|
|
|
ENST00000706955.1:c.*1179_*1181delinsGCT
|
ENSP00000516675.1:n.*1179_*1181delinsGCT
|
|
|
ENST00000686459.1:c.*730_*732delinsGCT
|
ENSP00000508909.1:n.*730_*732delinsGCT
|
|
|
ENST00000688158.1:c.*1255_*1257delinsGCT
|
ENSP00000509254.1:n.*1255_*1257delinsGCT
|
|
|
ENST00000688308.1:c.1144_1146delinsGCT
|
ENSP00000508752.1:p.Thr382Ala
|
|
|
ENST00000688922.1:c.1065_1067delinsGCT
|
|
|
|
ENST00000693560.1:c.1663_1665delinsGCT
|
ENSP00000509861.1:p.Thr555Ala
|
|
|
ENST00000371953.8:c.1144_1146delinsGCT
MANE Select
|
ENSP00000361021.3:p.Thr382Ala
|
|
|
ENST00000371953.7:c.1144_1146delinsGCT
|
ENSP00000361021.3:p.Thr382Ala
|
|
|
NM_000314.5:c.1144_1146delinsGCT
|
NP_000305.3:p.Thr382Ala
|
|
|
NM_000314.6:c.1144_1146delinsGCT
|
NP_000305.3:p.Thr382Ala
|
|
|
NM_001304717.2:c.1663_1665delinsGCT
|
NP_001291646.2:p.Thr555Ala
|
|
|
NM_001304718.1:c.553_555delinsGCT
|
NP_001291647.1:p.Thr185Ala
|
|
|
XM_006717926.2:c.1099_1101delinsGCT
|
XP_006717989.1:p.Thr367Ala
|
|
|
XM_011539982.1:c.1048_1050delinsGCT
|
XP_011538284.1:p.Thr350Ala
|
|
|
XR_945791.1:n.1714_1716delinsGCT
|
|
|
|
NM_000314.7:c.1144_1146delinsGCT
|
NP_000305.3:p.Thr382Ala
|
|
|
NM_001304717.5:c.1663_1665delinsGCT
|
NP_001291646.4:p.Thr555Ala
|
|
|
NM_001304718.2:c.553_555delinsGCT
|
NP_001291647.1:p.Thr185Ala
|
|
|
NM_000314.8:c.1144_1146delinsGCT
MANE Select
|
NP_000305.3:p.Thr382Ala
|
|
