ENST00000700029.2:c.733_735delinsTAT
|
ENSP00000514759.2:p.Gln245Tyr
|
|
ENST00000710265.1:c.733_735delinsTAT
|
ENSP00000518161.1:p.Gln245Tyr
|
|
ENST00000472832.3:c.733_735delinsTAT
|
ENSP00000483066.2:p.Gln245Tyr
|
|
ENST00000688158.2:n.1468_1470delinsTAT
|
|
|
ENST00000688922.2:c.*563_*565delinsTAT
|
ENSP00000508742.2:n.*563_*565delinsTAT
|
|
ENST00000700021.1:c.688_690delinsTAT
|
ENSP00000514757.1:p.Gln230Tyr
|
|
ENST00000700022.1:c.*72_*74delinsTAT
|
ENSP00000514758.1:n.*72_*74delinsTAT
|
|
ENST00000700023.1:n.1891_1893delinsTAT
|
|
|
ENST00000700024.1:n.2125_2127delinsTAT
|
|
|
ENST00000700025.1:n.1502_1504delinsTAT
|
|
|
ENST00000700026.1:n.370_372delinsTAT
|
|
|
ENST00000700029.1:c.567_569delinsTAT
|
|
|
ENST00000706954.1:c.733_735delinsTAT
|
ENSP00000516674.1:p.Gln245Tyr
|
|
ENST00000706955.1:c.*768_*770delinsTAT
|
ENSP00000516675.1:n.*768_*770delinsTAT
|
|
ENST00000686459.1:c.*319_*321delinsTAT
|
ENSP00000508909.1:n.*319_*321delinsTAT
|
|
ENST00000688158.1:c.*844_*846delinsTAT
|
ENSP00000509254.1:n.*844_*846delinsTAT
|
|
ENST00000688308.1:c.733_735delinsTAT
|
ENSP00000508752.1:p.Gln245Tyr
|
|
ENST00000688922.1:c.654_656delinsTAT
|
|
|
ENST00000693560.1:c.1252_1254delinsTAT
|
ENSP00000509861.1:p.Gln418Tyr
|
|
ENST00000371953.8:c.733_735delinsTAT
MANE Select
|
ENSP00000361021.3:p.Gln245Tyr
|
|
ENST00000371953.7:c.733_735delinsTAT
|
ENSP00000361021.3:p.Gln245Tyr
|
|
ENST00000472832.2:c.160_162delinsTAT
|
ENSP00000483066.1:p.Gln54Tyr
|
|
NM_000314.5:c.733_735delinsTAT
|
NP_000305.3:p.Gln245Tyr
|
|
NM_000314.6:c.733_735delinsTAT
|
NP_000305.3:p.Gln245Tyr
|
|
NM_001304717.2:c.1252_1254delinsTAT
|
NP_001291646.2:p.Gln418Tyr
|
|
NM_001304718.1:c.142_144delinsTAT
|
NP_001291647.1:p.Gln48Tyr
|
|
XM_006717926.2:c.688_690delinsTAT
|
XP_006717989.1:p.Gln230Tyr
|
|
XM_011539981.1:c.733_735delinsTAT
|
XP_011538283.1:p.Gln245Tyr
|
|
XM_011539982.1:c.637_639delinsTAT
|
XP_011538284.1:p.Gln213Tyr
|
|
XR_945791.1:n.1303_1305delinsTAT
|
|
|
NM_000314.7:c.733_735delinsTAT
|
NP_000305.3:p.Gln245Tyr
|
|
NM_001304717.5:c.1252_1254delinsTAT
|
NP_001291646.4:p.Gln418Tyr
|
|
NM_001304718.2:c.142_144delinsTAT
|
NP_001291647.1:p.Gln48Tyr
|
|
NM_000314.8:c.733_735delinsTAT
MANE Select
|
NP_000305.3:p.Gln245Tyr
|
|