ENST00000542672.7:c.2044G>A
|
ENSP00000443495.1:p.Glu682Lys
|
|
ENST00000461367.2:n.340G>A
|
|
|
ENST00000492634.7:n.1974G>A
|
|
|
ENST00000682015.1:c.1951G>A
|
ENSP00000506961.1:p.Glu651Lys
|
|
ENST00000682692.1:n.3139G>A
|
|
|
ENST00000682966.1:n.7685G>A
|
|
|
ENST00000683111.1:c.*1330G>A
|
ENSP00000507913.1:n.*1330G>A
|
|
ENST00000683322.1:n.3396G>A
|
|
|
ENST00000683805.1:n.835G>A
|
|
|
ENST00000684050.1:n.4682G>A
|
|
|
ENST00000684122.1:n.191G>A
|
|
|
ENST00000684286.1:n.3599G>A
|
|
|
ENST00000684502.1:n.3341G>A
|
|
|
ENST00000684763.1:n.659G>A
|
|
|
ENST00000366578.6:c.2044G>A
MANE Select
|
ENSP00000355537.4:p.Glu682Lys
|
|
ENST00000492634.6:n.1974G>A
|
|
|
ENST00000542672.6:c.2044G>A
|
ENSP00000443495.1:p.Glu682Lys
|
|
ENST00000651091.1:c.1734G>A
|
ENSP00000498677.1:n.1734G>A
|
|
ENST00000651275.1:c.1936G>A
|
ENSP00000498926.1:p.Glu646Lys
|
|
ENST00000651781.1:c.1124G>A
|
|
|
ENST00000651786.1:c.*1416G>A
|
ENSP00000498364.1:n.*1416G>A
|
|
ENST00000652096.1:c.*1449G>A
|
ENSP00000498896.1:n.*1449G>A
|
|
ENST00000366578.5:c.2044G>A
|
ENSP00000355537.4:p.Glu682Lys
|
|
ENST00000461367.1:n.253G>A
|
|
|
ENST00000542672.5:c.2044G>A
|
ENSP00000443495.1:p.Glu682Lys
|
|
ENST00000546208.5:c.1420G>A
|
ENSP00000438384.2:p.Glu474Lys
|
|
NM_001103.3:c.2044G>A
|
NP_001094.1:p.Glu682Lys
|
|
NM_001278343.1:c.2044G>A
|
NP_001265272.1:p.Glu682Lys
|
|
NM_001278344.1:c.1420G>A
|
NP_001265273.1:p.Glu474Lys
|
|
NM_001278343.2:c.2044G>A
|
NP_001265272.1:p.Glu682Lys
|
|
NM_001103.4:c.2044G>A
MANE Select
|
NP_001094.1:p.Glu682Lys
|
|
NM_001278344.2:c.1420G>A
|
NP_001265273.1:p.Glu474Lys
|
|