|
ENST00000689298.1:c.*3321G>T
|
ENSP00000508434.1:n.*3321G>T
|
|
|
ENST00000440875.6:c.2695G>T
|
ENSP00000475553.3:p.Glu899Ter
|
|
|
ENST00000627532.3:c.3472G>T
MANE Select
|
ENSP00000487174.1:p.Glu1158Ter
|
|
|
ENST00000636026.2:c.3360G>T
|
ENSP00000490776.1:p.Thr1120=
|
|
|
ENST00000636179.1:n.3441G>T
|
|
|
|
ENST00000636413.1:c.3136G>T
|
ENSP00000490508.1:p.Glu1046Ter
|
|
|
ENST00000636471.1:c.3547G>T
|
ENSP00000490317.1:p.Glu1183Ter
|
|
|
ENST00000636732.2:c.*3189G>T
|
ENSP00000490175.1:n.*3189G>T
|
|
|
ENST00000636820.1:n.3572G>T
|
|
|
|
ENST00000637045.1:c.3136G>T
|
ENSP00000490141.1:p.Glu1046Ter
|
|
|
ENST00000637304.1:c.3136G>T
|
ENSP00000490872.1:p.Glu1046Ter
|
|
|
ENST00000638007.1:c.3136G>T
|
ENSP00000490723.1:p.Glu1046Ter
|
|
|
ENST00000638087.1:c.3136G>T
|
ENSP00000490673.1:p.Glu1046Ter
|
|
|
ENST00000638128.1:c.2695G>T
|
ENSP00000490934.1:p.Glu899Ter
|
|
|
ENST00000639389.1:c.151+6788G>T
|
ENSP00000492572.1:n.151+6788G>T
|
|
|
ENST00000647488.1:c.692G>T
|
ENSP00000494820.1:n.692G>T
|
|
|
ENST00000675069.1:c.1003G>T
|
ENSP00000502467.1:p.Glu335Ter
|
|
|
ENST00000303660.8:c.3469G>T
|
ENSP00000302501.4:p.Glu1157Ter
|
|
|
ENST00000409487.7:c.3472G>T
|
ENSP00000386854.2:p.Glu1158Ter
|
|
|
ENST00000419938.5:c.656-742G>T
|
ENSP00000394777.2:n.656-742G>T
|
|
|
ENST00000539609.7:c.3400G>T
|
ENSP00000443792.2:p.Glu1134Ter
|
|
|
ENST00000558170.6:c.3472G>T
|
ENSP00000454157.1:p.Glu1158Ter
|
|
|
ENST00000627532.2:c.3472G>T
|
ENSP00000487174.1:p.Glu1158Ter
|
|
|
NM_001171653.1:c.3400G>T
|
NP_001165124.1:p.Glu1134Ter
|
|
|
NM_014795.3:c.3472G>T
|
NP_055610.1:p.Glu1158Ter
|
|
|
XM_006712881.2:c.3472G>T
|
XP_006712944.1:p.Glu1158Ter
|
|
|
XM_006712882.2:c.3472G>T
|
XP_006712945.1:p.Glu1158Ter
|
|
|
XM_011512231.1:c.3463G>T
|
XP_011510533.1:p.Glu1155Ter
|
|
|
XM_011512232.1:c.3451G>T
|
XP_011510534.1:p.Glu1151Ter
|
|
|
NM_014795.4:c.3472G>T
MANE Select
|
NP_055610.1:p.Glu1158Ter
|
|
|
NM_001171653.2:c.3400G>T
|
NP_001165124.1:p.Glu1134Ter
|
|
