|
ENST00000700029.2:c.796_798delinsTAT
|
ENSP00000514759.2:p.Lys266Tyr
|
|
|
ENST00000710265.1:c.796_798delinsTAT
|
ENSP00000518161.1:p.Lys266Tyr
|
|
|
ENST00000472832.3:c.796_798delinsTAT
|
ENSP00000483066.2:p.Lys266Tyr
|
|
|
ENST00000688158.2:n.1531_1533delinsTAT
|
|
|
|
ENST00000688922.2:c.*626_*628delinsTAT
|
ENSP00000508742.2:n.*626_*628delinsTAT
|
|
|
ENST00000700021.1:c.751_753delinsTAT
|
ENSP00000514757.1:p.Lys251Tyr
|
|
|
ENST00000700022.1:c.*135_*137delinsTAT
|
ENSP00000514758.1:n.*135_*137delinsTAT
|
|
|
ENST00000700023.1:n.1954_1956delinsTAT
|
|
|
|
ENST00000700024.1:n.2188_2190delinsTAT
|
|
|
|
ENST00000700025.1:n.1565_1567delinsTAT
|
|
|
|
ENST00000700026.1:n.433_435delinsTAT
|
|
|
|
ENST00000700029.1:c.630_632delinsTAT
|
|
|
|
ENST00000706954.1:c.796_798delinsTAT
|
ENSP00000516674.1:p.Lys266Tyr
|
|
|
ENST00000706955.1:c.*831_*833delinsTAT
|
ENSP00000516675.1:n.*831_*833delinsTAT
|
|
|
ENST00000686459.1:c.*382_*384delinsTAT
|
ENSP00000508909.1:n.*382_*384delinsTAT
|
|
|
ENST00000688158.1:c.*907_*909delinsTAT
|
ENSP00000509254.1:n.*907_*909delinsTAT
|
|
|
ENST00000688308.1:c.796_798delinsTAT
|
ENSP00000508752.1:p.Lys266Tyr
|
|
|
ENST00000688922.1:c.717_719delinsTAT
|
|
|
|
ENST00000693560.1:c.1315_1317delinsTAT
|
ENSP00000509861.1:p.Lys439Tyr
|
|
|
ENST00000371953.8:c.796_798delinsTAT
MANE Select
|
ENSP00000361021.3:p.Lys266Tyr
|
|
|
ENST00000371953.7:c.796_798delinsTAT
|
ENSP00000361021.3:p.Lys266Tyr
|
|
|
ENST00000472832.2:c.223_225delinsTAT
|
ENSP00000483066.1:p.Lys75Tyr
|
|
|
NM_000314.5:c.796_798delinsTAT
|
NP_000305.3:p.Lys266Tyr
|
|
|
NM_000314.6:c.796_798delinsTAT
|
NP_000305.3:p.Lys266Tyr
|
|
|
NM_001304717.2:c.1315_1317delinsTAT
|
NP_001291646.2:p.Lys439Tyr
|
|
|
NM_001304718.1:c.205_207delinsTAT
|
NP_001291647.1:p.Lys69Tyr
|
|
|
XM_006717926.2:c.751_753delinsTAT
|
XP_006717989.1:p.Lys251Tyr
|
|
|
XM_011539981.1:c.796_798delinsTAT
|
XP_011538283.1:p.Lys266Tyr
|
|
|
XM_011539982.1:c.700_702delinsTAT
|
XP_011538284.1:p.Lys234Tyr
|
|
|
XR_945791.1:n.1366_1368delinsTAT
|
|
|
|
NM_000314.7:c.796_798delinsTAT
|
NP_000305.3:p.Lys266Tyr
|
|
|
NM_001304717.5:c.1315_1317delinsTAT
|
NP_001291646.4:p.Lys439Tyr
|
|
|
NM_001304718.2:c.205_207delinsTAT
|
NP_001291647.1:p.Lys69Tyr
|
|
|
NM_000314.8:c.796_798delinsTAT
MANE Select
|
NP_000305.3:p.Lys266Tyr
|
|
