|
ENST00000689298.1:c.*2575T>A
|
ENSP00000508434.1:n.*2575T>A
|
|
|
ENST00000440875.6:c.1949T>A
|
ENSP00000475553.3:p.Phe650Tyr
|
|
|
ENST00000627532.3:c.2726T>A
MANE Select
|
ENSP00000487174.1:p.Phe909Tyr
|
|
|
ENST00000636026.2:c.2726T>A
|
ENSP00000490776.1:p.Phe909Tyr
|
|
|
ENST00000636179.1:n.2695T>A
|
|
|
|
ENST00000636413.1:c.2390T>A
|
ENSP00000490508.1:p.Phe797Tyr
|
|
|
ENST00000636471.1:c.2801T>A
|
ENSP00000490317.1:p.Phe934Tyr
|
|
|
ENST00000636732.2:c.*2443T>A
|
ENSP00000490175.1:n.*2443T>A
|
|
|
ENST00000636820.1:n.2826T>A
|
|
|
|
ENST00000637045.1:c.2390T>A
|
ENSP00000490141.1:p.Phe797Tyr
|
|
|
ENST00000637304.1:c.2390T>A
|
ENSP00000490872.1:p.Phe797Tyr
|
|
|
ENST00000638007.1:c.2390T>A
|
ENSP00000490723.1:p.Phe797Tyr
|
|
|
ENST00000638087.1:c.2390T>A
|
ENSP00000490673.1:p.Phe797Tyr
|
|
|
ENST00000638128.1:c.1949T>A
|
ENSP00000490934.1:p.Phe650Tyr
|
|
|
ENST00000675069.1:c.257T>A
|
ENSP00000502467.1:p.Phe86Tyr
|
|
|
ENST00000303660.8:c.2723T>A
|
ENSP00000302501.4:p.Phe908Tyr
|
|
|
ENST00000409487.7:c.2726T>A
|
ENSP00000386854.2:p.Phe909Tyr
|
|
|
ENST00000419938.5:c.655+2738T>A
|
ENSP00000394777.2:n.655+2738T>A
|
|
|
ENST00000440875.5:c.1168-533T>A
|
ENSP00000475553.2:n.1168-533T>A
|
|
|
ENST00000539609.7:c.2654T>A
|
ENSP00000443792.2:p.Phe885Tyr
|
|
|
ENST00000558170.6:c.2726T>A
|
ENSP00000454157.1:p.Phe909Tyr
|
|
|
ENST00000627532.2:c.2726T>A
|
ENSP00000487174.1:p.Phe909Tyr
|
|
|
NM_001171653.1:c.2654T>A
|
NP_001165124.1:p.Phe885Tyr
|
|
|
NM_014795.3:c.2726T>A
|
NP_055610.1:p.Phe909Tyr
|
|
|
XM_006712881.2:c.2726T>A
|
XP_006712944.1:p.Phe909Tyr
|
|
|
XM_006712882.2:c.2726T>A
|
XP_006712945.1:p.Phe909Tyr
|
|
|
XM_011512231.1:c.2717T>A
|
XP_011510533.1:p.Phe906Tyr
|
|
|
XM_011512232.1:c.2705T>A
|
XP_011510534.1:p.Phe902Tyr
|
|
|
NM_014795.4:c.2726T>A
MANE Select
|
NP_055610.1:p.Phe909Tyr
|
|
|
NM_001171653.2:c.2654T>A
|
NP_001165124.1:p.Phe885Tyr
|
|
