ENST00000703936.1:c.2855_2856insGTG
|
ENSP00000515567.1:p.Val952_Leu953insCys
|
|
ENST00000703937.1:c.*1916_*1917insGTG
|
ENSP00000515568.1:n.*1916_*1917insGTG
|
|
ENST00000326739.9:c.815_816insGTG
MANE Select
|
ENSP00000321584.4:p.Val272_Leu273insCys
|
|
ENST00000429182.6:c.815_816insGTG
|
ENSP00000393525.2:p.Val272_Leu273insCys
|
|
ENST00000442157.2:c.740_741insGTG
|
ENSP00000403502.2:p.Val247_Leu248insCys
|
|
ENST00000462980.2:n.1330_1331insGTG
|
|
|
ENST00000472328.2:n.881_882insGTG
|
|
|
ENST00000491610.2:n.775_776insGTG
|
|
|
ENST00000676607.1:n.1111_1112insGTG
|
|
|
ENST00000676627.1:n.1545_1546insGTG
|
|
|
ENST00000676708.1:n.2095_2096insGTG
|
|
|
ENST00000676864.1:n.1964_1965insGTG
|
|
|
ENST00000677010.1:c.851_852insGTG
|
ENSP00000503089.1:p.Val284_Leu285insCys
|
|
ENST00000677108.1:n.2721_2722insGTG
|
|
|
ENST00000677168.1:n.1287_1288insGTG
|
|
|
ENST00000677185.1:n.1378_1379insGTG
|
|
|
ENST00000677205.1:n.1599_1600insGTG
|
|
|
ENST00000677344.1:n.2089_2090insGTG
|
|
|
ENST00000677480.1:c.*492_*493insGTG
|
ENSP00000504378.1:n.*492_*493insGTG
|
|
ENST00000677519.1:n.1525_1526insGTG
|
|
|
ENST00000677593.1:n.1371_1372insGTG
|
|
|
ENST00000677740.1:n.2320_2321insGTG
|
|
|
ENST00000677991.1:n.1988_1989insGTG
|
|
|
ENST00000678001.1:n.1308_1309insGTG
|
|
|
ENST00000678085.1:n.1371_1372insGTG
|
|
|
ENST00000678177.1:n.2664_2665insGTG
|
|
|
ENST00000678603.1:n.1893_1894insGTG
|
|
|
ENST00000678724.1:c.740_741insGTG
|
ENSP00000503874.1:p.Val247_Leu248insCys
|
|
ENST00000678920.1:n.973_974insGTG
|
|
|
ENST00000679019.1:n.1585_1586insGTG
|
|
|
ENST00000679117.1:c.*630_*631insGTG
|
ENSP00000503240.1:n.*630_*631insGTG
|
|
ENST00000679339.1:n.1656_1657insGTG
|
|
|
ENST00000326739.8:c.815_816insGTG
|
ENSP00000321584.4:p.Val272_Leu273insCys
|
|
ENST00000429182.5:c.609_610insGTG
|
|
|
ENST00000442157.1:c.740_741insGTG
|
ENSP00000403502.1:p.Val247_Leu248insCys
|
|
ENST00000462980.1:n.717_718insGTG
|
|
|
ENST00000491610.1:n.775_776insGTG
|
|
|
NM_000884.2:c.815_816insGTG
|
NP_000875.2:p.Val272_Leu273insCys
|
|
XM_006713128.2:c.1025_1026insGTG
|
XP_006713191.1:p.Val342_Leu343insCys
|
|
XM_006713128.3:c.1025_1026insGTG
|
XP_006713191.1:p.Val342_Leu343insCys
|
|
XM_017006349.1:c.950_951insGTG
|
XP_016861838.1:p.Val317_Leu318insCys
|
|
XM_017006350.1:c.950_951insGTG
|
XP_016861839.1:p.Val317_Leu318insCys
|
|
NM_000884.3:c.815_816insGTG
MANE Select
|
NP_000875.2:p.Val272_Leu273insCys
|
|