|
ENST00000689298.1:c.*631_*632del
|
ENSP00000508434.1:n.*631_*632del
|
|
|
ENST00000440875.6:c.5_6del
|
ENSP00000475553.3:p.Val2AspfsTer18
|
|
|
ENST00000627532.3:c.782_783del
MANE Select
|
ENSP00000487174.1:p.Val261AspfsTer18
|
|
|
ENST00000636026.2:c.782_783del
|
ENSP00000490776.1:p.Val261AspfsTer18
|
|
|
ENST00000636179.1:n.751_752del
|
|
|
|
ENST00000636413.1:c.446_447del
|
ENSP00000490508.1:p.Val149AspfsTer18
|
|
|
ENST00000636471.1:c.782_783del
|
ENSP00000490317.1:p.Val261AspfsTer18
|
|
|
ENST00000636732.2:c.*499_*500del
|
ENSP00000490175.1:n.*499_*500del
|
|
|
ENST00000636820.1:n.882_883del
|
|
|
|
ENST00000637045.1:c.446_447del
|
ENSP00000490141.1:p.Val149AspfsTer18
|
|
|
ENST00000637267.2:c.782_783del
|
ENSP00000490293.2:p.Val261AspfsTer18
|
|
|
ENST00000637304.1:c.446_447del
|
ENSP00000490872.1:p.Val149AspfsTer18
|
|
|
ENST00000638007.1:c.446_447del
|
ENSP00000490723.1:p.Val149AspfsTer18
|
|
|
ENST00000638087.1:c.446_447del
|
ENSP00000490673.1:p.Val149AspfsTer18
|
|
|
ENST00000638128.1:c.5_6del
|
ENSP00000490934.1:p.Val2AspfsTer18
|
|
|
ENST00000675069.1:c.-133-5091_-133-5090del
|
ENSP00000502467.1:n.-133-5091_-133-5090del
|
|
|
ENST00000303660.8:c.779_780del
|
ENSP00000302501.4:p.Val260AspfsTer18
|
|
|
ENST00000392861.6:c.866_867del
|
ENSP00000376601.3:p.Val289AspfsTer18
|
|
|
ENST00000409487.7:c.782_783del
|
ENSP00000386854.2:p.Val261AspfsTer18
|
|
|
ENST00000419938.5:c.521_522del
|
ENSP00000394777.2:p.Val174AspfsTer18
|
|
|
ENST00000427902.5:c.869_870del
|
ENSP00000395496.2:p.Val290AspfsTer18
|
|
|
ENST00000440875.5:c.767_768del
|
ENSP00000475553.2:p.Val256AspfsTer18
|
|
|
ENST00000539609.7:c.710_711del
|
ENSP00000443792.2:p.Val237AspfsTer18
|
|
|
ENST00000558170.6:c.782_783del
|
ENSP00000454157.1:p.Val261AspfsTer18
|
|
|
ENST00000627532.2:c.782_783del
|
ENSP00000487174.1:p.Val261AspfsTer18
|
|
|
NM_001171653.1:c.710_711del
|
NP_001165124.1:p.Val237AspfsTer18
|
|
|
NM_014795.3:c.782_783del
|
NP_055610.1:p.Val261AspfsTer18
|
|
|
XM_006712881.2:c.782_783del
|
XP_006712944.1:p.Val261AspfsTer18
|
|
|
XM_006712882.2:c.782_783del
|
XP_006712945.1:p.Val261AspfsTer18
|
|
|
XM_011512231.1:c.773_774del
|
XP_011510533.1:p.Val258AspfsTer18
|
|
|
XM_011512232.1:c.761_762del
|
XP_011510534.1:p.Val254AspfsTer18
|
|
|
NM_014795.4:c.782_783del
MANE Select
|
NP_055610.1:p.Val261AspfsTer18
|
|
|
NM_001171653.2:c.710_711del
|
NP_001165124.1:p.Val237AspfsTer18
|
|
