ENST00000689298.1:c.*505_*506delinsGC
|
ENSP00000508434.1:n.*505_*506delinsGC
|
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ENST00000440875.6:c.-122_-121delinsGC
|
ENSP00000475553.3:n.-122_-121delinsGC
|
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ENST00000627532.3:c.656_657delinsGC
MANE Select
|
ENSP00000487174.1:p.Gly219=
|
|
ENST00000636026.2:c.656_657delinsGC
|
ENSP00000490776.1:p.Gly219=
|
|
ENST00000636179.1:n.625_626delinsGC
|
|
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ENST00000636413.1:c.320_321delinsGC
|
ENSP00000490508.1:p.Gly107=
|
|
ENST00000636471.1:c.656_657delinsGC
|
ENSP00000490317.1:p.Gly219=
|
|
ENST00000636732.2:c.*373_*374delinsGC
|
ENSP00000490175.1:n.*373_*374delinsGC
|
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ENST00000636820.1:n.756_757delinsGC
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|
|
ENST00000637045.1:c.320_321delinsGC
|
ENSP00000490141.1:p.Gly107=
|
|
ENST00000637267.2:c.656_657delinsGC
|
ENSP00000490293.2:p.Gly219=
|
|
ENST00000637304.1:c.320_321delinsGC
|
ENSP00000490872.1:p.Gly107=
|
|
ENST00000638007.1:c.320_321delinsGC
|
ENSP00000490723.1:p.Gly107=
|
|
ENST00000638087.1:c.320_321delinsGC
|
ENSP00000490673.1:p.Gly107=
|
|
ENST00000638128.1:c.-122_-121delinsGC
|
ENSP00000490934.1:n.-122_-121delinsGC
|
|
ENST00000675069.1:c.-133-5217_-133-5216delinsGC
|
ENSP00000502467.1:n.-133-5217_-133-5216de...
|
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ENST00000303660.8:c.653_654delinsGC
|
ENSP00000302501.4:p.Gly218=
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ENST00000392861.6:c.740_741delinsGC
|
ENSP00000376601.3:p.Gly247=
|
|
ENST00000409487.7:c.656_657delinsGC
|
ENSP00000386854.2:p.Gly219=
|
|
ENST00000419938.5:c.395_396delinsGC
|
ENSP00000394777.2:p.Gly132=
|
|
ENST00000427902.5:c.743_744delinsGC
|
ENSP00000395496.2:p.Gly248=
|
|
ENST00000440875.5:c.641_642delinsGC
|
ENSP00000475553.2:p.Gly214=
|
|
ENST00000497268.1:n.602_603delinsGC
|
|
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ENST00000539609.7:c.584_585delinsGC
|
ENSP00000443792.2:p.Gly195=
|
|
ENST00000558170.6:c.656_657delinsGC
|
ENSP00000454157.1:p.Gly219=
|
|
ENST00000627532.2:c.656_657delinsGC
|
ENSP00000487174.1:p.Gly219=
|
|
NM_001171653.1:c.584_585delinsGC
|
NP_001165124.1:p.Gly195=
|
|
NM_014795.3:c.656_657delinsGC
|
NP_055610.1:p.Gly219=
|
|
XM_006712881.2:c.656_657delinsGC
|
XP_006712944.1:p.Gly219=
|
|
XM_006712882.2:c.656_657delinsGC
|
XP_006712945.1:p.Gly219=
|
|
XM_011512231.1:c.647_648delinsGC
|
XP_011510533.1:p.Gly216=
|
|
XM_011512232.1:c.635_636delinsGC
|
XP_011510534.1:p.Gly212=
|
|
NM_014795.4:c.656_657delinsGC
MANE Select
|
NP_055610.1:p.Gly219=
|
|
NM_001171653.2:c.584_585delinsGC
|
NP_001165124.1:p.Gly195=
|
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