|
ENST00000689298.1:c.*1067A=
|
ENSP00000508434.1:n.*1067A=
|
|
|
ENST00000440875.6:c.441A=
|
ENSP00000475553.3:p.Thr147=
|
|
|
ENST00000627532.3:c.1218A=
MANE Select
|
ENSP00000487174.1:p.Thr406=
|
|
|
ENST00000636026.2:c.1218A=
|
ENSP00000490776.1:p.Thr406=
|
|
|
ENST00000636179.1:n.1187A=
|
|
|
|
ENST00000636413.1:c.882A=
|
ENSP00000490508.1:p.Thr294=
|
|
|
ENST00000636471.1:c.1293A=
|
ENSP00000490317.1:p.Thr431=
|
|
|
ENST00000636732.2:c.*935A=
|
ENSP00000490175.1:n.*935A=
|
|
|
ENST00000636820.1:n.1318A=
|
|
|
|
ENST00000637045.1:c.882A=
|
ENSP00000490141.1:p.Thr294=
|
|
|
ENST00000637267.2:c.1218A=
|
ENSP00000490293.2:p.Thr406=
|
|
|
ENST00000637304.1:c.882A=
|
ENSP00000490872.1:p.Thr294=
|
|
|
ENST00000638007.1:c.882A=
|
ENSP00000490723.1:p.Thr294=
|
|
|
ENST00000638087.1:c.882A=
|
ENSP00000490673.1:p.Thr294=
|
|
|
ENST00000638128.1:c.441A=
|
ENSP00000490934.1:p.Thr147=
|
|
|
ENST00000675069.1:c.-133-1119A=
|
ENSP00000502467.1:n.-133-1119A=
|
|
|
ENST00000675145.1:n.1766A=
|
|
|
|
ENST00000303660.8:c.1215A=
|
ENSP00000302501.4:p.Thr405=
|
|
|
ENST00000392861.6:c.1302A=
|
ENSP00000376601.3:p.Thr434=
|
|
|
ENST00000409487.7:c.1218A=
|
ENSP00000386854.2:p.Thr406=
|
|
|
ENST00000419938.5:c.655+1230A=
|
ENSP00000394777.2:n.655+1230A=
|
|
|
ENST00000427902.5:c.1305A=
|
ENSP00000395496.2:p.Thr435=
|
|
|
ENST00000440875.5:c.1153+50A=
|
ENSP00000475553.2:n.1153+50A=
|
|
|
ENST00000539609.7:c.1146A=
|
ENSP00000443792.2:p.Thr382=
|
|
|
ENST00000558170.6:c.1218A=
|
ENSP00000454157.1:p.Thr406=
|
|
|
ENST00000627532.2:c.1218A=
|
ENSP00000487174.1:p.Thr406=
|
|
|
NM_001171653.1:c.1146A=
|
NP_001165124.1:p.Thr382=
|
|
|
NM_014795.3:c.1218A=
|
NP_055610.1:p.Thr406=
|
|
|
XM_006712881.2:c.1218A=
|
XP_006712944.1:p.Thr406=
|
|
|
XM_006712882.2:c.1218A=
|
XP_006712945.1:p.Thr406=
|
|
|
XM_011512231.1:c.1209A=
|
XP_011510533.1:p.Thr403=
|
|
|
XM_011512232.1:c.1197A=
|
XP_011510534.1:p.Thr399=
|
|
|
NM_014795.4:c.1218A=
MANE Select
|
NP_055610.1:p.Thr406=
|
|
|
NM_001171653.2:c.1146A=
|
NP_001165124.1:p.Thr382=
|
|
