|
ENST00000689298.1:c.*3153G>T
|
ENSP00000508434.1:n.*3153G>T
|
|
|
ENST00000440875.6:c.2527G>T
|
ENSP00000475553.3:p.Glu843Ter
|
|
|
ENST00000627532.3:c.3304G>T
MANE Select
|
ENSP00000487174.1:p.Glu1102Ter
|
|
|
ENST00000636026.2:c.3231-39G>T
|
ENSP00000490776.1:n.3231-39G>T
|
|
|
ENST00000636179.1:n.3273G>T
|
|
|
|
ENST00000636413.1:c.2968G>T
|
ENSP00000490508.1:p.Glu990Ter
|
|
|
ENST00000636471.1:c.3379G>T
|
ENSP00000490317.1:p.Glu1127Ter
|
|
|
ENST00000636732.2:c.*3021G>T
|
ENSP00000490175.1:n.*3021G>T
|
|
|
ENST00000636820.1:n.3404G>T
|
|
|
|
ENST00000637045.1:c.2968G>T
|
ENSP00000490141.1:p.Glu990Ter
|
|
|
ENST00000637304.1:c.2968G>T
|
ENSP00000490872.1:p.Glu990Ter
|
|
|
ENST00000638007.1:c.2968G>T
|
ENSP00000490723.1:p.Glu990Ter
|
|
|
ENST00000638087.1:c.2968G>T
|
ENSP00000490673.1:p.Glu990Ter
|
|
|
ENST00000638128.1:c.2527G>T
|
ENSP00000490934.1:p.Glu843Ter
|
|
|
ENST00000639389.1:c.151+6620G>T
|
ENSP00000492572.1:n.151+6620G>T
|
|
|
ENST00000647488.1:c.524G>T
|
ENSP00000494820.1:n.524G>T
|
|
|
ENST00000675069.1:c.835G>T
|
ENSP00000502467.1:p.Glu279Ter
|
|
|
ENST00000303660.8:c.3301G>T
|
ENSP00000302501.4:p.Glu1101Ter
|
|
|
ENST00000409487.7:c.3304G>T
|
ENSP00000386854.2:p.Glu1102Ter
|
|
|
ENST00000419938.5:c.656-910G>T
|
ENSP00000394777.2:n.656-910G>T
|
|
|
ENST00000539609.7:c.3232G>T
|
ENSP00000443792.2:p.Glu1078Ter
|
|
|
ENST00000558170.6:c.3304G>T
|
ENSP00000454157.1:p.Glu1102Ter
|
|
|
ENST00000627532.2:c.3304G>T
|
ENSP00000487174.1:p.Glu1102Ter
|
|
|
NM_001171653.1:c.3232G>T
|
NP_001165124.1:p.Glu1078Ter
|
|
|
NM_014795.3:c.3304G>T
|
NP_055610.1:p.Glu1102Ter
|
|
|
XM_006712881.2:c.3304G>T
|
XP_006712944.1:p.Glu1102Ter
|
|
|
XM_006712882.2:c.3304G>T
|
XP_006712945.1:p.Glu1102Ter
|
|
|
XM_011512231.1:c.3295G>T
|
XP_011510533.1:p.Glu1099Ter
|
|
|
XM_011512232.1:c.3283G>T
|
XP_011510534.1:p.Glu1095Ter
|
|
|
NM_014795.4:c.3304G>T
MANE Select
|
NP_055610.1:p.Glu1102Ter
|
|
|
NM_001171653.2:c.3232G>T
|
NP_001165124.1:p.Glu1078Ter
|
|
