|
ENST00000700029.2:c.781_783delinsTAT
|
ENSP00000514759.2:p.Gln261Tyr
|
|
|
ENST00000710265.1:c.781_783delinsTAT
|
ENSP00000518161.1:p.Gln261Tyr
|
|
|
ENST00000472832.3:c.781_783delinsTAT
|
ENSP00000483066.2:p.Gln261Tyr
|
|
|
ENST00000688158.2:n.1516_1518delinsTAT
|
|
|
|
ENST00000688922.2:c.*611_*613delinsTAT
|
ENSP00000508742.2:n.*611_*613delinsTAT
|
|
|
ENST00000700021.1:c.736_738delinsTAT
|
ENSP00000514757.1:p.Gln246Tyr
|
|
|
ENST00000700022.1:c.*120_*122delinsTAT
|
ENSP00000514758.1:n.*120_*122delinsTAT
|
|
|
ENST00000700023.1:n.1939_1941delinsTAT
|
|
|
|
ENST00000700024.1:n.2173_2175delinsTAT
|
|
|
|
ENST00000700025.1:n.1550_1552delinsTAT
|
|
|
|
ENST00000700026.1:n.418_420delinsTAT
|
|
|
|
ENST00000700029.1:c.615_617delinsTAT
|
|
|
|
ENST00000706954.1:c.781_783delinsTAT
|
ENSP00000516674.1:p.Gln261Tyr
|
|
|
ENST00000706955.1:c.*816_*818delinsTAT
|
ENSP00000516675.1:n.*816_*818delinsTAT
|
|
|
ENST00000686459.1:c.*367_*369delinsTAT
|
ENSP00000508909.1:n.*367_*369delinsTAT
|
|
|
ENST00000688158.1:c.*892_*894delinsTAT
|
ENSP00000509254.1:n.*892_*894delinsTAT
|
|
|
ENST00000688308.1:c.781_783delinsTAT
|
ENSP00000508752.1:p.Gln261Tyr
|
|
|
ENST00000688922.1:c.702_704delinsTAT
|
|
|
|
ENST00000693560.1:c.1300_1302delinsTAT
|
ENSP00000509861.1:p.Gln434Tyr
|
|
|
ENST00000371953.8:c.781_783delinsTAT
MANE Select
|
ENSP00000361021.3:p.Gln261Tyr
|
|
|
ENST00000371953.7:c.781_783delinsTAT
|
ENSP00000361021.3:p.Gln261Tyr
|
|
|
ENST00000472832.2:c.208_210delinsTAT
|
ENSP00000483066.1:p.Gln70Tyr
|
|
|
NM_000314.5:c.781_783delinsTAT
|
NP_000305.3:p.Gln261Tyr
|
|
|
NM_000314.6:c.781_783delinsTAT
|
NP_000305.3:p.Gln261Tyr
|
|
|
NM_001304717.2:c.1300_1302delinsTAT
|
NP_001291646.2:p.Gln434Tyr
|
|
|
NM_001304718.1:c.190_192delinsTAT
|
NP_001291647.1:p.Gln64Tyr
|
|
|
XM_006717926.2:c.736_738delinsTAT
|
XP_006717989.1:p.Gln246Tyr
|
|
|
XM_011539981.1:c.781_783delinsTAT
|
XP_011538283.1:p.Gln261Tyr
|
|
|
XM_011539982.1:c.685_687delinsTAT
|
XP_011538284.1:p.Gln229Tyr
|
|
|
XR_945791.1:n.1351_1353delinsTAT
|
|
|
|
NM_000314.7:c.781_783delinsTAT
|
NP_000305.3:p.Gln261Tyr
|
|
|
NM_001304717.5:c.1300_1302delinsTAT
|
NP_001291646.4:p.Gln434Tyr
|
|
|
NM_001304718.2:c.190_192delinsTAT
|
NP_001291647.1:p.Gln64Tyr
|
|
|
NM_000314.8:c.781_783delinsTAT
MANE Select
|
NP_000305.3:p.Gln261Tyr
|
|
