ENST00000700029.2:c.1096_1098delinsTTT
|
ENSP00000514759.2:p.Arg366Phe
|
|
ENST00000710265.1:c.1003_1005delinsTTT
|
ENSP00000518161.1:p.Arg335Phe
|
|
ENST00000472832.3:c.1003_1005delinsTTT
|
ENSP00000483066.2:p.Arg335Phe
|
|
ENST00000688158.2:n.1738_1740delinsTTT
|
|
|
ENST00000688922.2:c.*833_*835delinsTTT
|
ENSP00000508742.2:n.*833_*835delinsTTT
|
|
ENST00000700021.1:c.958_960delinsTTT
|
ENSP00000514757.1:p.Arg320Phe
|
|
ENST00000700022.1:c.*342_*344delinsTTT
|
ENSP00000514758.1:n.*342_*344delinsTTT
|
|
ENST00000700023.1:n.2161_2163delinsTTT
|
|
|
ENST00000700024.1:n.2395_2397delinsTTT
|
|
|
ENST00000700025.1:n.1772_1774delinsTTT
|
|
|
ENST00000700026.1:n.640_642delinsTTT
|
|
|
ENST00000706954.1:c.1003_1005delinsTTT
|
ENSP00000516674.1:p.Arg335Phe
|
|
ENST00000706955.1:c.*1038_*1040delinsTTT
|
ENSP00000516675.1:n.*1038_*1040delinsTTT
|
|
ENST00000686459.1:c.*589_*591delinsTTT
|
ENSP00000508909.1:n.*589_*591delinsTTT
|
|
ENST00000688158.1:c.*1114_*1116delinsTTT
|
ENSP00000509254.1:n.*1114_*1116delinsTTT
|
|
ENST00000688308.1:c.1003_1005delinsTTT
|
ENSP00000508752.1:p.Arg335Phe
|
|
ENST00000688922.1:c.924_926delinsTTT
|
|
|
ENST00000693560.1:c.1522_1524delinsTTT
|
ENSP00000509861.1:p.Arg508Phe
|
|
ENST00000371953.8:c.1003_1005delinsTTT
MANE Select
|
ENSP00000361021.3:p.Arg335Phe
|
|
ENST00000371953.7:c.1003_1005delinsTTT
|
ENSP00000361021.3:p.Arg335Phe
|
|
ENST00000472832.2:c.430_432delinsTTT
|
ENSP00000483066.1:p.Arg144Phe
|
|
NM_000314.5:c.1003_1005delinsTTT
|
NP_000305.3:p.Arg335Phe
|
|
NM_000314.6:c.1003_1005delinsTTT
|
NP_000305.3:p.Arg335Phe
|
|
NM_001304717.2:c.1522_1524delinsTTT
|
NP_001291646.2:p.Arg508Phe
|
|
NM_001304718.1:c.412_414delinsTTT
|
NP_001291647.1:p.Arg138Phe
|
|
XM_006717926.2:c.958_960delinsTTT
|
XP_006717989.1:p.Arg320Phe
|
|
XM_011539981.1:c.1003_1005delinsTTT
|
XP_011538283.1:p.Arg335Phe
|
|
XM_011539982.1:c.907_909delinsTTT
|
XP_011538284.1:p.Arg303Phe
|
|
XR_945791.1:n.1573_1575delinsTTT
|
|
|
NM_000314.7:c.1003_1005delinsTTT
|
NP_000305.3:p.Arg335Phe
|
|
NM_001304717.5:c.1522_1524delinsTTT
|
NP_001291646.4:p.Arg508Phe
|
|
NM_001304718.2:c.412_414delinsTTT
|
NP_001291647.1:p.Arg138Phe
|
|
NM_000314.8:c.1003_1005delinsTTT
MANE Select
|
NP_000305.3:p.Arg335Phe
|
|