|
ENST00000689298.1:c.*3277A=
|
ENSP00000508434.1:n.*3277A=
|
|
|
ENST00000440875.6:c.2651A=
|
ENSP00000475553.3:p.Glu884=
|
|
|
ENST00000627532.3:c.3428A=
MANE Select
|
ENSP00000487174.1:p.Glu1143=
|
|
|
ENST00000636026.2:c.3316A=
|
ENSP00000490776.1:p.Lys1106=
|
|
|
ENST00000636179.1:n.3397A=
|
|
|
|
ENST00000636413.1:c.3092A=
|
ENSP00000490508.1:p.Glu1031=
|
|
|
ENST00000636471.1:c.3503A=
|
ENSP00000490317.1:p.Glu1168=
|
|
|
ENST00000636732.2:c.*3145A=
|
ENSP00000490175.1:n.*3145A=
|
|
|
ENST00000636820.1:n.3528A=
|
|
|
|
ENST00000637045.1:c.3092A=
|
ENSP00000490141.1:p.Glu1031=
|
|
|
ENST00000637304.1:c.3092A=
|
ENSP00000490872.1:p.Glu1031=
|
|
|
ENST00000638007.1:c.3092A=
|
ENSP00000490723.1:p.Glu1031=
|
|
|
ENST00000638087.1:c.3092A=
|
ENSP00000490673.1:p.Glu1031=
|
|
|
ENST00000638128.1:c.2651A=
|
ENSP00000490934.1:p.Glu884=
|
|
|
ENST00000639389.1:c.151+6744A=
|
ENSP00000492572.1:n.151+6744A=
|
|
|
ENST00000647488.1:c.648A=
|
ENSP00000494820.1:n.648A=
|
|
|
ENST00000675069.1:c.959A=
|
ENSP00000502467.1:p.Glu320=
|
|
|
ENST00000303660.8:c.3425A=
|
ENSP00000302501.4:p.Glu1142=
|
|
|
ENST00000409487.7:c.3428A=
|
ENSP00000386854.2:p.Glu1143=
|
|
|
ENST00000419938.5:c.656-786A=
|
ENSP00000394777.2:n.656-786A=
|
|
|
ENST00000539609.7:c.3356A=
|
ENSP00000443792.2:p.Glu1119=
|
|
|
ENST00000558170.6:c.3428A=
|
ENSP00000454157.1:p.Glu1143=
|
|
|
ENST00000627532.2:c.3428A=
|
ENSP00000487174.1:p.Glu1143=
|
|
|
NM_001171653.1:c.3356A=
|
NP_001165124.1:p.Glu1119=
|
|
|
NM_014795.3:c.3428A=
|
NP_055610.1:p.Glu1143=
|
|
|
XM_006712881.2:c.3428A=
|
XP_006712944.1:p.Glu1143=
|
|
|
XM_006712882.2:c.3428A=
|
XP_006712945.1:p.Glu1143=
|
|
|
XM_011512231.1:c.3419A=
|
XP_011510533.1:p.Glu1140=
|
|
|
XM_011512232.1:c.3407A=
|
XP_011510534.1:p.Glu1136=
|
|
|
NM_014795.4:c.3428A=
MANE Select
|
NP_055610.1:p.Glu1143=
|
|
|
NM_001171653.2:c.3356A=
|
NP_001165124.1:p.Glu1119=
|
|
