|
ENST00000700029.2:c.757_758delinsTA
|
ENSP00000514759.2:p.Ile253Tyr
|
|
|
ENST00000710265.1:c.757_758delinsTA
|
ENSP00000518161.1:p.Ile253Tyr
|
|
|
ENST00000472832.3:c.757_758delinsTA
|
ENSP00000483066.2:p.Ile253Tyr
|
|
|
ENST00000688158.2:n.1492_1493delinsTA
|
|
|
|
ENST00000688922.2:c.*587_*588delinsTA
|
ENSP00000508742.2:n.*587_*588delinsTA
|
|
|
ENST00000700021.1:c.712_713delinsTA
|
ENSP00000514757.1:p.Ile238Tyr
|
|
|
ENST00000700022.1:c.*96_*97delinsTA
|
ENSP00000514758.1:n.*96_*97delinsTA
|
|
|
ENST00000700023.1:n.1915_1916delinsTA
|
|
|
|
ENST00000700024.1:n.2149_2150delinsTA
|
|
|
|
ENST00000700025.1:n.1526_1527delinsTA
|
|
|
|
ENST00000700026.1:n.394_395delinsTA
|
|
|
|
ENST00000700029.1:c.591_592delinsTA
|
|
|
|
ENST00000706954.1:c.757_758delinsTA
|
ENSP00000516674.1:p.Ile253Tyr
|
|
|
ENST00000706955.1:c.*792_*793delinsTA
|
ENSP00000516675.1:n.*792_*793delinsTA
|
|
|
ENST00000686459.1:c.*343_*344delinsTA
|
ENSP00000508909.1:n.*343_*344delinsTA
|
|
|
ENST00000688158.1:c.*868_*869delinsTA
|
ENSP00000509254.1:n.*868_*869delinsTA
|
|
|
ENST00000688308.1:c.757_758delinsTA
|
ENSP00000508752.1:p.Ile253Tyr
|
|
|
ENST00000688922.1:c.678_679delinsTA
|
|
|
|
ENST00000693560.1:c.1276_1277delinsTA
|
ENSP00000509861.1:p.Ile426Tyr
|
|
|
ENST00000371953.8:c.757_758delinsTA
MANE Select
|
ENSP00000361021.3:p.Ile253Tyr
|
|
|
ENST00000371953.7:c.757_758delinsTA
|
ENSP00000361021.3:p.Ile253Tyr
|
|
|
ENST00000472832.2:c.184_185delinsTA
|
ENSP00000483066.1:p.Ile62Tyr
|
|
|
NM_000314.5:c.757_758delinsTA
|
NP_000305.3:p.Ile253Tyr
|
|
|
NM_000314.6:c.757_758delinsTA
|
NP_000305.3:p.Ile253Tyr
|
|
|
NM_001304717.2:c.1276_1277delinsTA
|
NP_001291646.2:p.Ile426Tyr
|
|
|
NM_001304718.1:c.166_167delinsTA
|
NP_001291647.1:p.Ile56Tyr
|
|
|
XM_006717926.2:c.712_713delinsTA
|
XP_006717989.1:p.Ile238Tyr
|
|
|
XM_011539981.1:c.757_758delinsTA
|
XP_011538283.1:p.Ile253Tyr
|
|
|
XM_011539982.1:c.661_662delinsTA
|
XP_011538284.1:p.Ile221Tyr
|
|
|
XR_945791.1:n.1327_1328delinsTA
|
|
|
|
NM_000314.7:c.757_758delinsTA
|
NP_000305.3:p.Ile253Tyr
|
|
|
NM_001304717.5:c.1276_1277delinsTA
|
NP_001291646.4:p.Ile426Tyr
|
|
|
NM_001304718.2:c.166_167delinsTA
|
NP_001291647.1:p.Ile56Tyr
|
|
|
NM_000314.8:c.757_758delinsTA
MANE Select
|
NP_000305.3:p.Ile253Tyr
|
|
