ENST00000320700.10:c.590A>T
MANE Select
|
ENSP00000316938.5:p.Asp197Val
|
|
ENST00000320700.9:c.590A>T
|
ENSP00000316938.5:p.Asp197Val
|
|
ENST00000382437.8:c.527A>T
|
ENSP00000371874.4:p.Asp176Val
|
|
ENST00000564065.5:c.590A>T
|
ENSP00000454562.1:p.Asp197Val
|
|
ENST00000567494.5:c.590A>T
|
ENSP00000455358.1:p.Asp197Val
|
|
ENST00000569184.1:c.581A>T
|
ENSP00000455478.1:p.Asp194Val
|
|
ENST00000613572.4:c.527A>T
|
ENSP00000482627.1:p.Asp176Val
|
|
NM_001301680.1:c.590A>T
|
NP_001288609.1:p.Asp197Val
|
|
NM_001374.2:c.590A>T
|
NP_001365.1:p.Asp197Val
|
|
XM_011522399.1:c.863A>T
|
XP_011520701.1:p.Asp288Val
|
|
XM_011522399.2:c.863A>T
|
XP_011520701.1:p.Asp288Val
|
|
NM_001374.3:c.590A>T
MANE Select
|
NP_001365.1:p.Asp197Val
|
|
NM_001301680.2:c.590A>T
|
NP_001288609.1:p.Asp197Val
|
|