|
ENST00000700029.2:c.785_786delinsCT
|
ENSP00000514759.2:p.Asn262Thr
|
|
|
ENST00000710265.1:c.785_786delinsCT
|
ENSP00000518161.1:p.Asn262Thr
|
|
|
ENST00000472832.3:c.785_786delinsCT
|
ENSP00000483066.2:p.Asn262Thr
|
|
|
ENST00000688158.2:n.1520_1521delinsCT
|
|
|
|
ENST00000688922.2:c.*615_*616delinsCT
|
ENSP00000508742.2:n.*615_*616delinsCT
|
|
|
ENST00000700021.1:c.740_741delinsCT
|
ENSP00000514757.1:p.Asn247Thr
|
|
|
ENST00000700022.1:c.*124_*125delinsCT
|
ENSP00000514758.1:n.*124_*125delinsCT
|
|
|
ENST00000700023.1:n.1943_1944delinsCT
|
|
|
|
ENST00000700024.1:n.2177_2178delinsCT
|
|
|
|
ENST00000700025.1:n.1554_1555delinsCT
|
|
|
|
ENST00000700026.1:n.422_423delinsCT
|
|
|
|
ENST00000700029.1:c.619_620delinsCT
|
|
|
|
ENST00000706954.1:c.785_786delinsCT
|
ENSP00000516674.1:p.Asn262Thr
|
|
|
ENST00000706955.1:c.*820_*821delinsCT
|
ENSP00000516675.1:n.*820_*821delinsCT
|
|
|
ENST00000686459.1:c.*371_*372delinsCT
|
ENSP00000508909.1:n.*371_*372delinsCT
|
|
|
ENST00000688158.1:c.*896_*897delinsCT
|
ENSP00000509254.1:n.*896_*897delinsCT
|
|
|
ENST00000688308.1:c.785_786delinsCT
|
ENSP00000508752.1:p.Asn262Thr
|
|
|
ENST00000688922.1:c.706_707delinsCT
|
|
|
|
ENST00000693560.1:c.1304_1305delinsCT
|
ENSP00000509861.1:p.Asn435Thr
|
|
|
ENST00000371953.8:c.785_786delinsCT
MANE Select
|
ENSP00000361021.3:p.Asn262Thr
|
|
|
ENST00000371953.7:c.785_786delinsCT
|
ENSP00000361021.3:p.Asn262Thr
|
|
|
ENST00000472832.2:c.212_213delinsCT
|
ENSP00000483066.1:p.Asn71Thr
|
|
|
NM_000314.5:c.785_786delinsCT
|
NP_000305.3:p.Asn262Thr
|
|
|
NM_000314.6:c.785_786delinsCT
|
NP_000305.3:p.Asn262Thr
|
|
|
NM_001304717.2:c.1304_1305delinsCT
|
NP_001291646.2:p.Asn435Thr
|
|
|
NM_001304718.1:c.194_195delinsCT
|
NP_001291647.1:p.Asn65Thr
|
|
|
XM_006717926.2:c.740_741delinsCT
|
XP_006717989.1:p.Asn247Thr
|
|
|
XM_011539981.1:c.785_786delinsCT
|
XP_011538283.1:p.Asn262Thr
|
|
|
XM_011539982.1:c.689_690delinsCT
|
XP_011538284.1:p.Asn230Thr
|
|
|
XR_945791.1:n.1355_1356delinsCT
|
|
|
|
NM_000314.7:c.785_786delinsCT
|
NP_000305.3:p.Asn262Thr
|
|
|
NM_001304717.5:c.1304_1305delinsCT
|
NP_001291646.4:p.Asn435Thr
|
|
|
NM_001304718.2:c.194_195delinsCT
|
NP_001291647.1:p.Asn65Thr
|
|
|
NM_000314.8:c.785_786delinsCT
MANE Select
|
NP_000305.3:p.Asn262Thr
|
|
