ENST00000689298.1:c.*631_*633delinsTGA
|
ENSP00000508434.1:n.*631_*633delinsTGA
|
|
ENST00000440875.6:c.5_7delinsTGA
|
ENSP00000475553.3:p.Val2=
|
|
ENST00000627532.3:c.782_784delinsTGA
MANE Select
|
ENSP00000487174.1:p.Val261=
|
|
ENST00000636026.2:c.782_784delinsTGA
|
ENSP00000490776.1:p.Val261=
|
|
ENST00000636179.1:n.751_753delinsTGA
|
|
|
ENST00000636413.1:c.446_448delinsTGA
|
ENSP00000490508.1:p.Val149=
|
|
ENST00000636471.1:c.782_784delinsTGA
|
ENSP00000490317.1:p.Val261=
|
|
ENST00000636732.2:c.*499_*501delinsTGA
|
ENSP00000490175.1:n.*499_*501delinsTGA
|
|
ENST00000636820.1:n.882_884delinsTGA
|
|
|
ENST00000637045.1:c.446_448delinsTGA
|
ENSP00000490141.1:p.Val149=
|
|
ENST00000637267.2:c.782_784delinsTGA
|
ENSP00000490293.2:p.Val261=
|
|
ENST00000637304.1:c.446_448delinsTGA
|
ENSP00000490872.1:p.Val149=
|
|
ENST00000638007.1:c.446_448delinsTGA
|
ENSP00000490723.1:p.Val149=
|
|
ENST00000638087.1:c.446_448delinsTGA
|
ENSP00000490673.1:p.Val149=
|
|
ENST00000638128.1:c.5_7delinsTGA
|
ENSP00000490934.1:p.Val2=
|
|
ENST00000675069.1:c.-133-5091_-133-5089delinsTGA
|
ENSP00000502467.1:n.-133-5091_-133-5089delinsTGA
|
|
ENST00000303660.8:c.779_781delinsTGA
|
ENSP00000302501.4:p.Val260=
|
|
ENST00000392861.6:c.866_868delinsTGA
|
ENSP00000376601.3:p.Val289=
|
|
ENST00000409487.7:c.782_784delinsTGA
|
ENSP00000386854.2:p.Val261=
|
|
ENST00000419938.5:c.521_523delinsTGA
|
ENSP00000394777.2:p.Val174=
|
|
ENST00000427902.5:c.869_871delinsTGA
|
ENSP00000395496.2:p.Val290=
|
|
ENST00000440875.5:c.767_769delinsTGA
|
ENSP00000475553.2:p.Val256=
|
|
ENST00000539609.7:c.710_712delinsTGA
|
ENSP00000443792.2:p.Val237=
|
|
ENST00000558170.6:c.782_784delinsTGA
|
ENSP00000454157.1:p.Val261=
|
|
ENST00000627532.2:c.782_784delinsTGA
|
ENSP00000487174.1:p.Val261=
|
|
NM_001171653.1:c.710_712delinsTGA
|
NP_001165124.1:p.Val237=
|
|
NM_014795.3:c.782_784delinsTGA
|
NP_055610.1:p.Val261=
|
|
XM_006712881.2:c.782_784delinsTGA
|
XP_006712944.1:p.Val261=
|
|
XM_006712882.2:c.782_784delinsTGA
|
XP_006712945.1:p.Val261=
|
|
XM_011512231.1:c.773_775delinsTGA
|
XP_011510533.1:p.Val258=
|
|
XM_011512232.1:c.761_763delinsTGA
|
XP_011510534.1:p.Val254=
|
|
NM_014795.4:c.782_784delinsTGA
MANE Select
|
NP_055610.1:p.Val261=
|
|
NM_001171653.2:c.710_712delinsTGA
|
NP_001165124.1:p.Val237=
|
|