ENST00000700029.2:c.1095_1096delinsTT
|
ENSP00000514759.2:p.Asn366Ter
|
|
ENST00000710265.1:c.1002_1003delinsTT
|
ENSP00000518161.1:p.Asn335Ter
|
|
ENST00000472832.3:c.1002_1003delinsTT
|
ENSP00000483066.2:p.Asn335Ter
|
|
ENST00000688158.2:n.1737_1738delinsTT
|
|
|
ENST00000688922.2:c.*832_*833delinsTT
|
ENSP00000508742.2:n.*832_*833delinsTT
|
|
ENST00000700021.1:c.957_958delinsTT
|
ENSP00000514757.1:p.Asn320Ter
|
|
ENST00000700022.1:c.*341_*342delinsTT
|
ENSP00000514758.1:n.*341_*342delinsTT
|
|
ENST00000700023.1:n.2160_2161delinsTT
|
|
|
ENST00000700024.1:n.2394_2395delinsTT
|
|
|
ENST00000700025.1:n.1771_1772delinsTT
|
|
|
ENST00000700026.1:n.639_640delinsTT
|
|
|
ENST00000706954.1:c.1002_1003delinsTT
|
ENSP00000516674.1:p.Asn335Ter
|
|
ENST00000706955.1:c.*1037_*1038delinsTT
|
ENSP00000516675.1:n.*1037_*1038delinsTT
|
|
ENST00000686459.1:c.*588_*589delinsTT
|
ENSP00000508909.1:n.*588_*589delinsTT
|
|
ENST00000688158.1:c.*1113_*1114delinsTT
|
ENSP00000509254.1:n.*1113_*1114delinsTT
|
|
ENST00000688308.1:c.1002_1003delinsTT
|
ENSP00000508752.1:p.Asn335Ter
|
|
ENST00000688922.1:c.923_924delinsTT
|
|
|
ENST00000693560.1:c.1521_1522delinsTT
|
ENSP00000509861.1:p.Asn508Ter
|
|
ENST00000371953.8:c.1002_1003delinsTT
MANE Select
|
ENSP00000361021.3:p.Asn335Ter
|
|
ENST00000371953.7:c.1002_1003delinsTT
|
ENSP00000361021.3:p.Asn335Ter
|
|
ENST00000472832.2:c.429_430delinsTT
|
ENSP00000483066.1:p.Asn144Ter
|
|
NM_000314.5:c.1002_1003delinsTT
|
NP_000305.3:p.Asn335Ter
|
|
NM_000314.6:c.1002_1003delinsTT
|
NP_000305.3:p.Asn335Ter
|
|
NM_001304717.2:c.1521_1522delinsTT
|
NP_001291646.2:p.Asn508Ter
|
|
NM_001304718.1:c.411_412delinsTT
|
NP_001291647.1:p.Asn138Ter
|
|
XM_006717926.2:c.957_958delinsTT
|
XP_006717989.1:p.Asn320Ter
|
|
XM_011539981.1:c.1002_1003delinsTT
|
XP_011538283.1:p.Asn335Ter
|
|
XM_011539982.1:c.906_907delinsTT
|
XP_011538284.1:p.Asn303Ter
|
|
XR_945791.1:n.1572_1573delinsTT
|
|
|
NM_000314.7:c.1002_1003delinsTT
|
NP_000305.3:p.Asn335Ter
|
|
NM_001304717.5:c.1521_1522delinsTT
|
NP_001291646.4:p.Asn508Ter
|
|
NM_001304718.2:c.411_412delinsTT
|
NP_001291647.1:p.Asn138Ter
|
|
NM_000314.8:c.1002_1003delinsTT
MANE Select
|
NP_000305.3:p.Asn335Ter
|
|