|
ENST00000700029.2:c.761_762delinsCT
|
ENSP00000514759.2:p.Lys254Thr
|
|
|
ENST00000710265.1:c.761_762delinsCT
|
ENSP00000518161.1:p.Lys254Thr
|
|
|
ENST00000472832.3:c.761_762delinsCT
|
ENSP00000483066.2:p.Lys254Thr
|
|
|
ENST00000688158.2:n.1496_1497delinsCT
|
|
|
|
ENST00000688922.2:c.*591_*592delinsCT
|
ENSP00000508742.2:n.*591_*592delinsCT
|
|
|
ENST00000700021.1:c.716_717delinsCT
|
ENSP00000514757.1:p.Lys239Thr
|
|
|
ENST00000700022.1:c.*100_*101delinsCT
|
ENSP00000514758.1:n.*100_*101delinsCT
|
|
|
ENST00000700023.1:n.1919_1920delinsCT
|
|
|
|
ENST00000700024.1:n.2153_2154delinsCT
|
|
|
|
ENST00000700025.1:n.1530_1531delinsCT
|
|
|
|
ENST00000700026.1:n.398_399delinsCT
|
|
|
|
ENST00000700029.1:c.595_596delinsCT
|
|
|
|
ENST00000706954.1:c.761_762delinsCT
|
ENSP00000516674.1:p.Lys254Thr
|
|
|
ENST00000706955.1:c.*796_*797delinsCT
|
ENSP00000516675.1:n.*796_*797delinsCT
|
|
|
ENST00000686459.1:c.*347_*348delinsCT
|
ENSP00000508909.1:n.*347_*348delinsCT
|
|
|
ENST00000688158.1:c.*872_*873delinsCT
|
ENSP00000509254.1:n.*872_*873delinsCT
|
|
|
ENST00000688308.1:c.761_762delinsCT
|
ENSP00000508752.1:p.Lys254Thr
|
|
|
ENST00000688922.1:c.682_683delinsCT
|
|
|
|
ENST00000693560.1:c.1280_1281delinsCT
|
ENSP00000509861.1:p.Lys427Thr
|
|
|
ENST00000371953.8:c.761_762delinsCT
MANE Select
|
ENSP00000361021.3:p.Lys254Thr
|
|
|
ENST00000371953.7:c.761_762delinsCT
|
ENSP00000361021.3:p.Lys254Thr
|
|
|
ENST00000472832.2:c.188_189delinsCT
|
ENSP00000483066.1:p.Lys63Thr
|
|
|
NM_000314.5:c.761_762delinsCT
|
NP_000305.3:p.Lys254Thr
|
|
|
NM_000314.6:c.761_762delinsCT
|
NP_000305.3:p.Lys254Thr
|
|
|
NM_001304717.2:c.1280_1281delinsCT
|
NP_001291646.2:p.Lys427Thr
|
|
|
NM_001304718.1:c.170_171delinsCT
|
NP_001291647.1:p.Lys57Thr
|
|
|
XM_006717926.2:c.716_717delinsCT
|
XP_006717989.1:p.Lys239Thr
|
|
|
XM_011539981.1:c.761_762delinsCT
|
XP_011538283.1:p.Lys254Thr
|
|
|
XM_011539982.1:c.665_666delinsCT
|
XP_011538284.1:p.Lys222Thr
|
|
|
XR_945791.1:n.1331_1332delinsCT
|
|
|
|
NM_000314.7:c.761_762delinsCT
|
NP_000305.3:p.Lys254Thr
|
|
|
NM_001304717.5:c.1280_1281delinsCT
|
NP_001291646.4:p.Lys427Thr
|
|
|
NM_001304718.2:c.170_171delinsCT
|
NP_001291647.1:p.Lys57Thr
|
|
|
NM_000314.8:c.761_762delinsCT
MANE Select
|
NP_000305.3:p.Lys254Thr
|
|
