ENST00000689298.1:c.*3366G>T
|
ENSP00000508434.1:n.*3366G>T
|
|
ENST00000440875.6:c.2740G>T
|
ENSP00000475553.3:p.Asp914Tyr
|
|
ENST00000627532.3:c.3517G>T
MANE Select
|
ENSP00000487174.1:p.Asp1173Tyr
|
|
ENST00000636026.2:c.3405G>T
|
ENSP00000490776.1:p.Trp1135Cys
|
|
ENST00000636179.1:n.3486G>T
|
|
|
ENST00000636413.1:c.3181G>T
|
ENSP00000490508.1:p.Asp1061Tyr
|
|
ENST00000636471.1:c.3592G>T
|
ENSP00000490317.1:p.Asp1198Tyr
|
|
ENST00000636732.2:c.*3234G>T
|
ENSP00000490175.1:n.*3234G>T
|
|
ENST00000636820.1:n.3617G>T
|
|
|
ENST00000637045.1:c.3181G>T
|
ENSP00000490141.1:p.Asp1061Tyr
|
|
ENST00000637304.1:c.3181G>T
|
ENSP00000490872.1:p.Asp1061Tyr
|
|
ENST00000638007.1:c.3181G>T
|
ENSP00000490723.1:p.Asp1061Tyr
|
|
ENST00000638087.1:c.3181G>T
|
ENSP00000490673.1:p.Asp1061Tyr
|
|
ENST00000638128.1:c.2740G>T
|
ENSP00000490934.1:p.Asp914Tyr
|
|
ENST00000639389.1:c.151+6833G>T
|
ENSP00000492572.1:n.151+6833G>T
|
|
ENST00000647488.1:c.737G>T
|
ENSP00000494820.1:n.737G>T
|
|
ENST00000675069.1:c.1048G>T
|
ENSP00000502467.1:p.Asp350Tyr
|
|
ENST00000303660.8:c.3514G>T
|
ENSP00000302501.4:p.Asp1172Tyr
|
|
ENST00000409487.7:c.3517G>T
|
ENSP00000386854.2:p.Asp1173Tyr
|
|
ENST00000419938.5:c.656-697G>T
|
ENSP00000394777.2:n.656-697G>T
|
|
ENST00000539609.7:c.3445G>T
|
ENSP00000443792.2:p.Asp1149Tyr
|
|
ENST00000558170.6:c.3517G>T
|
ENSP00000454157.1:p.Asp1173Tyr
|
|
ENST00000627532.2:c.3517G>T
|
ENSP00000487174.1:p.Asp1173Tyr
|
|
NM_001171653.1:c.3445G>T
|
NP_001165124.1:p.Asp1149Tyr
|
|
NM_014795.3:c.3517G>T
|
NP_055610.1:p.Asp1173Tyr
|
|
XM_006712881.2:c.3517G>T
|
XP_006712944.1:p.Asp1173Tyr
|
|
XM_006712882.2:c.3517G>T
|
XP_006712945.1:p.Asp1173Tyr
|
|
XM_011512231.1:c.3508G>T
|
XP_011510533.1:p.Asp1170Tyr
|
|
XM_011512232.1:c.3496G>T
|
XP_011510534.1:p.Asp1166Tyr
|
|
NM_014795.4:c.3517G>T
MANE Select
|
NP_055610.1:p.Asp1173Tyr
|
|
NM_001171653.2:c.3445G>T
|
NP_001165124.1:p.Asp1149Tyr
|
|