ENST00000689298.1:c.*2590_*2593dup
|
ENSP00000508434.1:n.*2590_*2593dup
|
|
ENST00000440875.6:c.1964_1967dup
|
ENSP00000475553.3:p.Ser657AspfsTer?
|
|
ENST00000627532.3:c.2741_2744dup
MANE Select
|
ENSP00000487174.1:p.Ser916AspfsTer?
|
|
ENST00000636026.2:c.2741_2744dup
|
ENSP00000490776.1:p.Ser916AspfsTer?
|
|
ENST00000636179.1:n.2710_2713dup
|
|
|
ENST00000636413.1:c.2405_2408dup
|
ENSP00000490508.1:p.Ser804AspfsTer?
|
|
ENST00000636471.1:c.2816_2819dup
|
ENSP00000490317.1:p.Ser941AspfsTer?
|
|
ENST00000636732.2:c.*2458_*2461dup
|
ENSP00000490175.1:n.*2458_*2461dup
|
|
ENST00000636820.1:n.2841_2844dup
|
|
|
ENST00000637045.1:c.2405_2408dup
|
ENSP00000490141.1:p.Ser804AspfsTer?
|
|
ENST00000637304.1:c.2405_2408dup
|
ENSP00000490872.1:p.Ser804AspfsTer?
|
|
ENST00000638007.1:c.2405_2408dup
|
ENSP00000490723.1:p.Ser804AspfsTer?
|
|
ENST00000638087.1:c.2405_2408dup
|
ENSP00000490673.1:p.Ser804AspfsTer?
|
|
ENST00000638128.1:c.1964_1967dup
|
ENSP00000490934.1:p.Ser657AspfsTer?
|
|
ENST00000675069.1:c.272_275dup
|
ENSP00000502467.1:p.Ser93AspfsTer?
|
|
ENST00000303660.8:c.2738_2741dup
|
ENSP00000302501.4:p.Ser915AspfsTer?
|
|
ENST00000409487.7:c.2741_2744dup
|
ENSP00000386854.2:p.Ser916AspfsTer?
|
|
ENST00000419938.5:c.655+2753_655+2756dup
|
ENSP00000394777.2:n.655+2753_655+2756dup
|
|
ENST00000440875.5:c.1168-518_1168-515dup
|
ENSP00000475553.2:n.1168-518_1168-515dup
|
|
ENST00000539609.7:c.2669_2672dup
|
ENSP00000443792.2:p.Ser892AspfsTer?
|
|
ENST00000558170.6:c.2741_2744dup
|
ENSP00000454157.1:p.Ser916AspfsTer?
|
|
ENST00000627532.2:c.2741_2744dup
|
ENSP00000487174.1:p.Ser916AspfsTer?
|
|
NM_001171653.1:c.2669_2672dup
|
NP_001165124.1:p.Ser892AspfsTer?
|
|
NM_014795.3:c.2741_2744dup
|
NP_055610.1:p.Ser916AspfsTer?
|
|
XM_006712881.2:c.2741_2744dup
|
XP_006712944.1:p.Ser916AspfsTer?
|
|
XM_006712882.2:c.2741_2744dup
|
XP_006712945.1:p.Ser916AspfsTer?
|
|
XM_011512231.1:c.2732_2735dup
|
XP_011510533.1:p.Ser913AspfsTer?
|
|
XM_011512232.1:c.2720_2723dup
|
XP_011510534.1:p.Ser909AspfsTer?
|
|
NM_014795.4:c.2741_2744dup
MANE Select
|
NP_055610.1:p.Ser916AspfsTer?
|
|
NM_001171653.2:c.2669_2672dup
|
NP_001165124.1:p.Ser892AspfsTer?
|
|