ENST00000689298.1:c.*1723_*1724insG
|
ENSP00000508434.1:n.*1723_*1724insG
|
|
ENST00000440875.6:c.1097_1098insG
|
ENSP00000475553.3:p.Gly367ArgfsTer5
|
|
ENST00000627532.3:c.1874_1875insG
MANE Select
|
ENSP00000487174.1:p.Gly626ArgfsTer5
|
|
ENST00000636026.2:c.1874_1875insG
|
ENSP00000490776.1:p.Gly626ArgfsTer5
|
|
ENST00000636179.1:n.1843_1844insG
|
|
|
ENST00000636413.1:c.1538_1539insG
|
ENSP00000490508.1:p.Gly514ArgfsTer5
|
|
ENST00000636471.1:c.1949_1950insG
|
ENSP00000490317.1:p.Gly651ArgfsTer5
|
|
ENST00000636732.2:c.*1591_*1592insG
|
ENSP00000490175.1:n.*1591_*1592insG
|
|
ENST00000636820.1:n.1974_1975insG
|
|
|
ENST00000637045.1:c.1538_1539insG
|
ENSP00000490141.1:p.Gly514ArgfsTer5
|
|
ENST00000637304.1:c.1538_1539insG
|
ENSP00000490872.1:p.Gly514ArgfsTer5
|
|
ENST00000638007.1:c.1538_1539insG
|
ENSP00000490723.1:p.Gly514ArgfsTer5
|
|
ENST00000638087.1:c.1538_1539insG
|
ENSP00000490673.1:p.Gly514ArgfsTer5
|
|
ENST00000638128.1:c.1097_1098insG
|
ENSP00000490934.1:p.Gly367ArgfsTer5
|
|
ENST00000675069.1:c.-133-463_-133-462insG
|
ENSP00000502467.1:n.-133-463_-133-462insG
|
|
ENST00000675145.1:n.2422_2423insG
|
|
|
ENST00000303660.8:c.1871_1872insG
|
ENSP00000302501.4:p.Gly625ArgfsTer5
|
|
ENST00000409487.7:c.1874_1875insG
|
ENSP00000386854.2:p.Gly626ArgfsTer5
|
|
ENST00000419938.5:c.655+1886_655+1887insG
|
ENSP00000394777.2:n.655+1886_655+1887insG
|
|
ENST00000427902.5:c.1961_1962insG
|
ENSP00000395496.2:p.Gly655ArgfsTer5
|
|
ENST00000440875.5:c.1167+224_1167+225insG
|
ENSP00000475553.2:n.1167+224_1167+225insG
|
|
ENST00000539609.7:c.1802_1803insG
|
ENSP00000443792.2:p.Gly602ArgfsTer5
|
|
ENST00000558170.6:c.1874_1875insG
|
ENSP00000454157.1:p.Gly626ArgfsTer5
|
|
ENST00000627532.2:c.1874_1875insG
|
ENSP00000487174.1:p.Gly626ArgfsTer5
|
|
NM_001171653.1:c.1802_1803insG
|
NP_001165124.1:p.Gly602ArgfsTer5
|
|
NM_014795.3:c.1874_1875insG
|
NP_055610.1:p.Gly626ArgfsTer5
|
|
XM_006712881.2:c.1874_1875insG
|
XP_006712944.1:p.Gly626ArgfsTer5
|
|
XM_006712882.2:c.1874_1875insG
|
XP_006712945.1:p.Gly626ArgfsTer5
|
|
XM_011512231.1:c.1865_1866insG
|
XP_011510533.1:p.Gly623ArgfsTer5
|
|
XM_011512232.1:c.1853_1854insG
|
XP_011510534.1:p.Gly619ArgfsTer5
|
|
NM_014795.4:c.1874_1875insG
MANE Select
|
NP_055610.1:p.Gly626ArgfsTer5
|
|
NM_001171653.2:c.1802_1803insG
|
NP_001165124.1:p.Gly602ArgfsTer5
|
|