ENST00000700029.2:c.922_924delinsTGT
|
ENSP00000514759.2:p.Thr308Cys
|
|
ENST00000710265.1:c.829_831delinsTGT
|
ENSP00000518161.1:p.Thr277Cys
|
|
ENST00000472832.3:c.829_831delinsTGT
|
ENSP00000483066.2:p.Thr277Cys
|
|
ENST00000688158.2:n.1564_1566delinsTGT
|
|
|
ENST00000688922.2:c.*659_*661delinsTGT
|
ENSP00000508742.2:n.*659_*661delinsTGT
|
|
ENST00000700021.1:c.784_786delinsTGT
|
ENSP00000514757.1:p.Thr262Cys
|
|
ENST00000700022.1:c.*168_*170delinsTGT
|
ENSP00000514758.1:n.*168_*170delinsTGT
|
|
ENST00000700023.1:n.1987_1989delinsTGT
|
|
|
ENST00000700024.1:n.2221_2223delinsTGT
|
|
|
ENST00000700025.1:n.1598_1600delinsTGT
|
|
|
ENST00000700026.1:n.466_468delinsTGT
|
|
|
ENST00000700029.1:c.756_758delinsTGT
|
|
|
ENST00000706954.1:c.829_831delinsTGT
|
ENSP00000516674.1:p.Thr277Cys
|
|
ENST00000706955.1:c.*864_*866delinsTGT
|
ENSP00000516675.1:n.*864_*866delinsTGT
|
|
ENST00000686459.1:c.*415_*417delinsTGT
|
ENSP00000508909.1:n.*415_*417delinsTGT
|
|
ENST00000688158.1:c.*940_*942delinsTGT
|
ENSP00000509254.1:n.*940_*942delinsTGT
|
|
ENST00000688308.1:c.829_831delinsTGT
|
ENSP00000508752.1:p.Thr277Cys
|
|
ENST00000688922.1:c.750_752delinsTGT
|
|
|
ENST00000693560.1:c.1348_1350delinsTGT
|
ENSP00000509861.1:p.Thr450Cys
|
|
ENST00000371953.8:c.829_831delinsTGT
MANE Select
|
ENSP00000361021.3:p.Thr277Cys
|
|
ENST00000371953.7:c.829_831delinsTGT
|
ENSP00000361021.3:p.Thr277Cys
|
|
ENST00000472832.2:c.256_258delinsTGT
|
ENSP00000483066.1:p.Thr86Cys
|
|
NM_000314.5:c.829_831delinsTGT
|
NP_000305.3:p.Thr277Cys
|
|
NM_000314.6:c.829_831delinsTGT
|
NP_000305.3:p.Thr277Cys
|
|
NM_001304717.2:c.1348_1350delinsTGT
|
NP_001291646.2:p.Thr450Cys
|
|
NM_001304718.1:c.238_240delinsTGT
|
NP_001291647.1:p.Thr80Cys
|
|
XM_006717926.2:c.784_786delinsTGT
|
XP_006717989.1:p.Thr262Cys
|
|
XM_011539981.1:c.829_831delinsTGT
|
XP_011538283.1:p.Thr277Cys
|
|
XM_011539982.1:c.733_735delinsTGT
|
XP_011538284.1:p.Thr245Cys
|
|
XR_945791.1:n.1399_1401delinsTGT
|
|
|
NM_000314.7:c.829_831delinsTGT
|
NP_000305.3:p.Thr277Cys
|
|
NM_001304717.5:c.1348_1350delinsTGT
|
NP_001291646.4:p.Thr450Cys
|
|
NM_001304718.2:c.238_240delinsTGT
|
NP_001291647.1:p.Thr80Cys
|
|
NM_000314.8:c.829_831delinsTGT
MANE Select
|
NP_000305.3:p.Thr277Cys
|
|