ENST00000689298.1:c.*442-59T>C
|
ENSP00000508434.1:n.*442-59T>C
|
|
ENST00000440875.6:c.-185-59T>C
|
ENSP00000475553.3:n.-185-59T>C
|
|
ENST00000627532.3:c.593-59T>C
MANE Select
|
ENSP00000487174.1:n.593-59T>C
|
|
ENST00000636026.2:c.593-59T>C
|
ENSP00000490776.1:n.593-59T>C
|
|
ENST00000636179.1:n.562-59T>C
|
|
|
ENST00000636413.1:c.257-59T>C
|
ENSP00000490508.1:n.257-59T>C
|
|
ENST00000636471.1:c.593-59T>C
|
ENSP00000490317.1:n.593-59T>C
|
|
ENST00000636732.2:c.*310-59T>C
|
ENSP00000490175.1:n.*310-59T>C
|
|
ENST00000636820.1:n.693-59T>C
|
|
|
ENST00000637045.1:c.257-59T>C
|
ENSP00000490141.1:n.257-59T>C
|
|
ENST00000637267.2:c.593-59T>C
|
ENSP00000490293.2:n.593-59T>C
|
|
ENST00000637304.1:c.257-59T>C
|
ENSP00000490872.1:n.257-59T>C
|
|
ENST00000638007.1:c.257-59T>C
|
ENSP00000490723.1:n.257-59T>C
|
|
ENST00000638087.1:c.257-59T>C
|
ENSP00000490673.1:n.257-59T>C
|
|
ENST00000638128.1:c.-185-59T>C
|
ENSP00000490934.1:n.-185-59T>C
|
|
ENST00000675069.1:c.-133-5339T>C
|
ENSP00000502467.1:n.-133-5339T>C
|
|
ENST00000303660.8:c.590-59T>C
|
ENSP00000302501.4:n.590-59T>C
|
|
ENST00000392861.6:c.677-59T>C
|
ENSP00000376601.3:n.677-59T>C
|
|
ENST00000409487.7:c.593-59T>C
|
ENSP00000386854.2:n.593-59T>C
|
|
ENST00000419938.5:c.332-59T>C
|
ENSP00000394777.2:n.332-59T>C
|
|
ENST00000427902.5:c.680-59T>C
|
ENSP00000395496.2:n.680-59T>C
|
|
ENST00000431672.4:c.521-59T>C
|
ENSP00000475267.2:n.521-59T>C
|
|
ENST00000440875.5:c.578-59T>C
|
ENSP00000475553.2:n.578-59T>C
|
|
ENST00000497268.1:n.539-59T>C
|
|
|
ENST00000539609.7:c.521-59T>C
|
ENSP00000443792.2:n.521-59T>C
|
|
ENST00000558170.6:c.593-59T>C
|
ENSP00000454157.1:n.593-59T>C
|
|
ENST00000627532.2:c.593-59T>C
|
ENSP00000487174.1:n.593-59T>C
|
|
ENST00000627856.2:n.553-59T>C
|
|
|
NM_001171653.1:c.521-59T>C
|
NP_001165124.1:n.521-59T>C
|
|
NM_014795.3:c.593-59T>C
|
NP_055610.1:n.593-59T>C
|
|
XM_006712881.2:c.593-59T>C
|
XP_006712944.1:n.593-59T>C
|
|
XM_006712882.2:c.593-59T>C
|
XP_006712945.1:n.593-59T>C
|
|
XM_011512231.1:c.584-59T>C
|
XP_011510533.1:n.584-59T>C
|
|
XM_011512232.1:c.572-59T>C
|
XP_011510534.1:n.572-59T>C
|
|
NM_014795.4:c.593-59T>C
MANE Select
|
NP_055610.1:n.593-59T>C
|
|
NM_001171653.2:c.521-59T>C
|
NP_001165124.1:n.521-59T>C
|
|