|
ENST00000700029.2:c.779_780delinsCT
|
ENSP00000514759.2:p.Lys260Thr
|
|
|
ENST00000710265.1:c.779_780delinsCT
|
ENSP00000518161.1:p.Lys260Thr
|
|
|
ENST00000472832.3:c.779_780delinsCT
|
ENSP00000483066.2:p.Lys260Thr
|
|
|
ENST00000688158.2:n.1514_1515delinsCT
|
|
|
|
ENST00000688922.2:c.*609_*610delinsCT
|
ENSP00000508742.2:n.*609_*610delinsCT
|
|
|
ENST00000700021.1:c.734_735delinsCT
|
ENSP00000514757.1:p.Lys245Thr
|
|
|
ENST00000700022.1:c.*118_*119delinsCT
|
ENSP00000514758.1:n.*118_*119delinsCT
|
|
|
ENST00000700023.1:n.1937_1938delinsCT
|
|
|
|
ENST00000700024.1:n.2171_2172delinsCT
|
|
|
|
ENST00000700025.1:n.1548_1549delinsCT
|
|
|
|
ENST00000700026.1:n.416_417delinsCT
|
|
|
|
ENST00000700029.1:c.613_614delinsCT
|
|
|
|
ENST00000706954.1:c.779_780delinsCT
|
ENSP00000516674.1:p.Lys260Thr
|
|
|
ENST00000706955.1:c.*814_*815delinsCT
|
ENSP00000516675.1:n.*814_*815delinsCT
|
|
|
ENST00000686459.1:c.*365_*366delinsCT
|
ENSP00000508909.1:n.*365_*366delinsCT
|
|
|
ENST00000688158.1:c.*890_*891delinsCT
|
ENSP00000509254.1:n.*890_*891delinsCT
|
|
|
ENST00000688308.1:c.779_780delinsCT
|
ENSP00000508752.1:p.Lys260Thr
|
|
|
ENST00000688922.1:c.700_701delinsCT
|
|
|
|
ENST00000693560.1:c.1298_1299delinsCT
|
ENSP00000509861.1:p.Lys433Thr
|
|
|
ENST00000371953.8:c.779_780delinsCT
MANE Select
|
ENSP00000361021.3:p.Lys260Thr
|
|
|
ENST00000371953.7:c.779_780delinsCT
|
ENSP00000361021.3:p.Lys260Thr
|
|
|
ENST00000472832.2:c.206_207delinsCT
|
ENSP00000483066.1:p.Lys69Thr
|
|
|
NM_000314.5:c.779_780delinsCT
|
NP_000305.3:p.Lys260Thr
|
|
|
NM_000314.6:c.779_780delinsCT
|
NP_000305.3:p.Lys260Thr
|
|
|
NM_001304717.2:c.1298_1299delinsCT
|
NP_001291646.2:p.Lys433Thr
|
|
|
NM_001304718.1:c.188_189delinsCT
|
NP_001291647.1:p.Lys63Thr
|
|
|
XM_006717926.2:c.734_735delinsCT
|
XP_006717989.1:p.Lys245Thr
|
|
|
XM_011539981.1:c.779_780delinsCT
|
XP_011538283.1:p.Lys260Thr
|
|
|
XM_011539982.1:c.683_684delinsCT
|
XP_011538284.1:p.Lys228Thr
|
|
|
XR_945791.1:n.1349_1350delinsCT
|
|
|
|
NM_000314.7:c.779_780delinsCT
|
NP_000305.3:p.Lys260Thr
|
|
|
NM_001304717.5:c.1298_1299delinsCT
|
NP_001291646.4:p.Lys433Thr
|
|
|
NM_001304718.2:c.188_189delinsCT
|
NP_001291647.1:p.Lys63Thr
|
|
|
NM_000314.8:c.779_780delinsCT
MANE Select
|
NP_000305.3:p.Lys260Thr
|
|
