ENST00000700029.2:c.760_762delinsTAT
|
ENSP00000514759.2:p.Lys254Tyr
|
|
ENST00000710265.1:c.760_762delinsTAT
|
ENSP00000518161.1:p.Lys254Tyr
|
|
ENST00000472832.3:c.760_762delinsTAT
|
ENSP00000483066.2:p.Lys254Tyr
|
|
ENST00000688158.2:n.1495_1497delinsTAT
|
|
|
ENST00000688922.2:c.*590_*592delinsTAT
|
ENSP00000508742.2:n.*590_*592delinsTAT
|
|
ENST00000700021.1:c.715_717delinsTAT
|
ENSP00000514757.1:p.Lys239Tyr
|
|
ENST00000700022.1:c.*99_*101delinsTAT
|
ENSP00000514758.1:n.*99_*101delinsTAT
|
|
ENST00000700023.1:n.1918_1920delinsTAT
|
|
|
ENST00000700024.1:n.2152_2154delinsTAT
|
|
|
ENST00000700025.1:n.1529_1531delinsTAT
|
|
|
ENST00000700026.1:n.397_399delinsTAT
|
|
|
ENST00000700029.1:c.594_596delinsTAT
|
|
|
ENST00000706954.1:c.760_762delinsTAT
|
ENSP00000516674.1:p.Lys254Tyr
|
|
ENST00000706955.1:c.*795_*797delinsTAT
|
ENSP00000516675.1:n.*795_*797delinsTAT
|
|
ENST00000686459.1:c.*346_*348delinsTAT
|
ENSP00000508909.1:n.*346_*348delinsTAT
|
|
ENST00000688158.1:c.*871_*873delinsTAT
|
ENSP00000509254.1:n.*871_*873delinsTAT
|
|
ENST00000688308.1:c.760_762delinsTAT
|
ENSP00000508752.1:p.Lys254Tyr
|
|
ENST00000688922.1:c.681_683delinsTAT
|
|
|
ENST00000693560.1:c.1279_1281delinsTAT
|
ENSP00000509861.1:p.Lys427Tyr
|
|
ENST00000371953.8:c.760_762delinsTAT
MANE Select
|
ENSP00000361021.3:p.Lys254Tyr
|
|
ENST00000371953.7:c.760_762delinsTAT
|
ENSP00000361021.3:p.Lys254Tyr
|
|
ENST00000472832.2:c.187_189delinsTAT
|
ENSP00000483066.1:p.Lys63Tyr
|
|
NM_000314.5:c.760_762delinsTAT
|
NP_000305.3:p.Lys254Tyr
|
|
NM_000314.6:c.760_762delinsTAT
|
NP_000305.3:p.Lys254Tyr
|
|
NM_001304717.2:c.1279_1281delinsTAT
|
NP_001291646.2:p.Lys427Tyr
|
|
NM_001304718.1:c.169_171delinsTAT
|
NP_001291647.1:p.Lys57Tyr
|
|
XM_006717926.2:c.715_717delinsTAT
|
XP_006717989.1:p.Lys239Tyr
|
|
XM_011539981.1:c.760_762delinsTAT
|
XP_011538283.1:p.Lys254Tyr
|
|
XM_011539982.1:c.664_666delinsTAT
|
XP_011538284.1:p.Lys222Tyr
|
|
XR_945791.1:n.1330_1332delinsTAT
|
|
|
NM_000314.7:c.760_762delinsTAT
|
NP_000305.3:p.Lys254Tyr
|
|
NM_001304717.5:c.1279_1281delinsTAT
|
NP_001291646.4:p.Lys427Tyr
|
|
NM_001304718.2:c.169_171delinsTAT
|
NP_001291647.1:p.Lys57Tyr
|
|
NM_000314.8:c.760_762delinsTAT
MANE Select
|
NP_000305.3:p.Lys254Tyr
|
|