ENST00000309755.9:c.1115A>T
MANE Select
|
ENSP00000312397.4:p.Asp372Val
|
|
ENST00000309755.8:c.1115A>T
|
ENSP00000312397.4:p.Asp372Val
|
|
ENST00000502381.1:n.702A>T
|
|
|
ENST00000504208.5:c.*335-10620A>T
|
ENSP00000423585.1:n.*335-10620A>T
|
|
ENST00000505853.1:c.995A>T
|
ENSP00000426173.1:p.Asp332Val
|
|
ENST00000506491.5:c.869A>T
|
ENSP00000424828.1:p.Asp290Val
|
|
ENST00000506873.5:n.740A>T
|
|
|
ENST00000508657.5:c.1019A>T
|
ENSP00000422099.1:p.Asp340Val
|
|
NM_001257194.1:c.1019A>T
|
NP_001244123.1:p.Asp340Val
|
|
NM_001257195.1:c.869A>T
|
NP_001244124.1:p.Asp290Val
|
|
NM_017415.2:c.1115A>T
|
NP_059111.2:p.Asp372Val
|
|
NM_017415.3:c.1115A>T
MANE Select
|
NP_059111.2:p.Asp372Val
|
|
NM_001257195.2:c.869A>T
|
NP_001244124.1:p.Asp290Val
|
|