ENST00000438257.9:c.523G>T
MANE Select
|
ENSP00000405854.5:p.Asp175Tyr
|
|
ENST00000555750.2:c.*361G>T
|
ENSP00000450980.2:n.*361G>T
|
|
ENST00000422005.7:c.*324G>T
|
ENSP00000411438.4:n.*324G>T
|
|
ENST00000438257.8:c.523G>T
|
ENSP00000405854.4:p.Asp175Tyr
|
|
ENST00000555750.1:c.631G>T
|
ENSP00000450980.1:p.Asp211Tyr
|
|
ENST00000555844.1:c.607G>T
|
|
|
ENST00000556811.5:c.499G>T
|
|
|
ENST00000557010.5:c.523G>T
|
ENSP00000451419.1:p.Asp175Tyr
|
|
ENST00000557125.1:c.147G>T
|
ENSP00000450547.1:p.Gly49=
|
|
NM_000793.5:c.523G>T
|
NP_000784.2:p.Asp175Tyr
|
|
NM_001007023.3:c.631G>T
|
NP_001007024.1:p.Asp211Tyr
|
|
NM_001242502.1:c.*324G>T
|
NP_001229431.1:n.*324G>T
|
|
NM_001242503.1:c.*324G>T
|
NP_001229432.1:n.*324G>T
|
|
NM_013989.4:c.523G>T
|
NP_054644.1:p.Asp175Tyr
|
|
NM_000793.6:c.523G>T
|
NP_000784.3:p.Asp175Tyr
|
|
NM_001324462.2:c.523G>T
|
NP_001311391.2:p.Asp175Tyr
|
|
NM_001366496.1:c.523G>T
|
NP_001353425.1:p.Asp175Tyr
|
|
NM_013989.5:c.523G>T
MANE Select
|
NP_054644.1:p.Asp175Tyr
|
|
NR_158990.1:n.663G>T
|
|
|
NR_158991.1:n.797G>T
|
|
|