|
ENST00000700029.2:c.758_759delinsCT
|
ENSP00000514759.2:p.Ile253Thr
|
|
|
ENST00000710265.1:c.758_759delinsCT
|
ENSP00000518161.1:p.Ile253Thr
|
|
|
ENST00000472832.3:c.758_759delinsCT
|
ENSP00000483066.2:p.Ile253Thr
|
|
|
ENST00000688158.2:n.1493_1494delinsCT
|
|
|
|
ENST00000688922.2:c.*588_*589delinsCT
|
ENSP00000508742.2:n.*588_*589delinsCT
|
|
|
ENST00000700021.1:c.713_714delinsCT
|
ENSP00000514757.1:p.Ile238Thr
|
|
|
ENST00000700022.1:c.*97_*98delinsCT
|
ENSP00000514758.1:n.*97_*98delinsCT
|
|
|
ENST00000700023.1:n.1916_1917delinsCT
|
|
|
|
ENST00000700024.1:n.2150_2151delinsCT
|
|
|
|
ENST00000700025.1:n.1527_1528delinsCT
|
|
|
|
ENST00000700026.1:n.395_396delinsCT
|
|
|
|
ENST00000700029.1:c.592_593delinsCT
|
|
|
|
ENST00000706954.1:c.758_759delinsCT
|
ENSP00000516674.1:p.Ile253Thr
|
|
|
ENST00000706955.1:c.*793_*794delinsCT
|
ENSP00000516675.1:n.*793_*794delinsCT
|
|
|
ENST00000686459.1:c.*344_*345delinsCT
|
ENSP00000508909.1:n.*344_*345delinsCT
|
|
|
ENST00000688158.1:c.*869_*870delinsCT
|
ENSP00000509254.1:n.*869_*870delinsCT
|
|
|
ENST00000688308.1:c.758_759delinsCT
|
ENSP00000508752.1:p.Ile253Thr
|
|
|
ENST00000688922.1:c.679_680delinsCT
|
|
|
|
ENST00000693560.1:c.1277_1278delinsCT
|
ENSP00000509861.1:p.Ile426Thr
|
|
|
ENST00000371953.8:c.758_759delinsCT
MANE Select
|
ENSP00000361021.3:p.Ile253Thr
|
|
|
ENST00000371953.7:c.758_759delinsCT
|
ENSP00000361021.3:p.Ile253Thr
|
|
|
ENST00000472832.2:c.185_186delinsCT
|
ENSP00000483066.1:p.Ile62Thr
|
|
|
NM_000314.5:c.758_759delinsCT
|
NP_000305.3:p.Ile253Thr
|
|
|
NM_000314.6:c.758_759delinsCT
|
NP_000305.3:p.Ile253Thr
|
|
|
NM_001304717.2:c.1277_1278delinsCT
|
NP_001291646.2:p.Ile426Thr
|
|
|
NM_001304718.1:c.167_168delinsCT
|
NP_001291647.1:p.Ile56Thr
|
|
|
XM_006717926.2:c.713_714delinsCT
|
XP_006717989.1:p.Ile238Thr
|
|
|
XM_011539981.1:c.758_759delinsCT
|
XP_011538283.1:p.Ile253Thr
|
|
|
XM_011539982.1:c.662_663delinsCT
|
XP_011538284.1:p.Ile221Thr
|
|
|
XR_945791.1:n.1328_1329delinsCT
|
|
|
|
NM_000314.7:c.758_759delinsCT
|
NP_000305.3:p.Ile253Thr
|
|
|
NM_001304717.5:c.1277_1278delinsCT
|
NP_001291646.4:p.Ile426Thr
|
|
|
NM_001304718.2:c.167_168delinsCT
|
NP_001291647.1:p.Ile56Thr
|
|
|
NM_000314.8:c.758_759delinsCT
MANE Select
|
NP_000305.3:p.Ile253Thr
|
|
