|
ENST00000700029.2:c.797_798delinsCT
|
ENSP00000514759.2:p.Lys266Thr
|
|
|
ENST00000710265.1:c.797_798delinsCT
|
ENSP00000518161.1:p.Lys266Thr
|
|
|
ENST00000472832.3:c.797_798delinsCT
|
ENSP00000483066.2:p.Lys266Thr
|
|
|
ENST00000688158.2:n.1532_1533delinsCT
|
|
|
|
ENST00000688922.2:c.*627_*628delinsCT
|
ENSP00000508742.2:n.*627_*628delinsCT
|
|
|
ENST00000700021.1:c.752_753delinsCT
|
ENSP00000514757.1:p.Lys251Thr
|
|
|
ENST00000700022.1:c.*136_*137delinsCT
|
ENSP00000514758.1:n.*136_*137delinsCT
|
|
|
ENST00000700023.1:n.1955_1956delinsCT
|
|
|
|
ENST00000700024.1:n.2189_2190delinsCT
|
|
|
|
ENST00000700025.1:n.1566_1567delinsCT
|
|
|
|
ENST00000700026.1:n.434_435delinsCT
|
|
|
|
ENST00000700029.1:c.631_632delinsCT
|
|
|
|
ENST00000706954.1:c.797_798delinsCT
|
ENSP00000516674.1:p.Lys266Thr
|
|
|
ENST00000706955.1:c.*832_*833delinsCT
|
ENSP00000516675.1:n.*832_*833delinsCT
|
|
|
ENST00000686459.1:c.*383_*384delinsCT
|
ENSP00000508909.1:n.*383_*384delinsCT
|
|
|
ENST00000688158.1:c.*908_*909delinsCT
|
ENSP00000509254.1:n.*908_*909delinsCT
|
|
|
ENST00000688308.1:c.797_798delinsCT
|
ENSP00000508752.1:p.Lys266Thr
|
|
|
ENST00000688922.1:c.718_719delinsCT
|
|
|
|
ENST00000693560.1:c.1316_1317delinsCT
|
ENSP00000509861.1:p.Lys439Thr
|
|
|
ENST00000371953.8:c.797_798delinsCT
MANE Select
|
ENSP00000361021.3:p.Lys266Thr
|
|
|
ENST00000371953.7:c.797_798delinsCT
|
ENSP00000361021.3:p.Lys266Thr
|
|
|
ENST00000472832.2:c.224_225delinsCT
|
ENSP00000483066.1:p.Lys75Thr
|
|
|
NM_000314.5:c.797_798delinsCT
|
NP_000305.3:p.Lys266Thr
|
|
|
NM_000314.6:c.797_798delinsCT
|
NP_000305.3:p.Lys266Thr
|
|
|
NM_001304717.2:c.1316_1317delinsCT
|
NP_001291646.2:p.Lys439Thr
|
|
|
NM_001304718.1:c.206_207delinsCT
|
NP_001291647.1:p.Lys69Thr
|
|
|
XM_006717926.2:c.752_753delinsCT
|
XP_006717989.1:p.Lys251Thr
|
|
|
XM_011539981.1:c.797_798delinsCT
|
XP_011538283.1:p.Lys266Thr
|
|
|
XM_011539982.1:c.701_702delinsCT
|
XP_011538284.1:p.Lys234Thr
|
|
|
XR_945791.1:n.1367_1368delinsCT
|
|
|
|
NM_000314.7:c.797_798delinsCT
|
NP_000305.3:p.Lys266Thr
|
|
|
NM_001304717.5:c.1316_1317delinsCT
|
NP_001291646.4:p.Lys439Thr
|
|
|
NM_001304718.2:c.206_207delinsCT
|
NP_001291647.1:p.Lys69Thr
|
|
|
NM_000314.8:c.797_798delinsCT
MANE Select
|
NP_000305.3:p.Lys266Thr
|
|
