ENST00000361740.9:c.816A>T
|
ENSP00000354468.5:p.Lys272Asn
|
|
ENST00000402438.6:c.615A>T
|
ENSP00000385679.1:p.Lys205Asn
|
|
ENST00000407332.6:c.702A>T
|
ENSP00000384457.2:p.Lys234Asn
|
|
ENST00000407623.8:c.615A>T
|
ENSP00000384834.3:p.Lys205Asn
|
|
ENST00000617178.5:c.221A>T
|
|
|
ENST00000684963.1:n.2424A>T
|
|
|
ENST00000685184.1:n.276A>T
|
|
|
ENST00000686523.1:c.*633A>T
|
ENSP00000508940.1:n.*633A>T
|
|
ENST00000687183.1:n.960A>T
|
|
|
ENST00000687198.1:c.615A>T
|
ENSP00000508492.1:p.Lys205Asn
|
|
ENST00000688117.1:c.783A>T
|
ENSP00000509015.1:p.Lys261Asn
|
|
ENST00000688244.1:c.384A>T
|
ENSP00000510355.1:p.Lys128Asn
|
|
ENST00000689001.1:n.1306A>T
|
|
|
ENST00000689195.1:c.600A>T
|
ENSP00000509895.1:p.Lys200Asn
|
|
ENST00000689239.1:n.851A>T
|
|
|
ENST00000689795.1:n.945A>T
|
|
|
ENST00000690835.1:c.*63A>T
|
ENSP00000509038.1:n.*63A>T
|
|
ENST00000690993.1:n.1439A>T
|
|
|
ENST00000691295.1:c.*167A>T
|
ENSP00000508706.1:n.*167A>T
|
|
ENST00000691918.1:c.974A>T
|
ENSP00000509525.1:n.974A>T
|
|
ENST00000692152.1:c.615A>T
|
ENSP00000509317.1:p.Lys205Asn
|
|
ENST00000692344.1:n.1171A>T
|
|
|
ENST00000693363.1:c.726A>T
|
ENSP00000510411.1:p.Lys242Asn
|
|
ENST00000693367.1:c.684A>T
|
ENSP00000508815.1:p.Lys228Asn
|
|
ENST00000693639.1:c.677A>T
|
ENSP00000510223.1:n.677A>T
|
|
ENST00000693646.1:c.590A>T
|
ENSP00000508449.1:n.590A>T
|
|
ENST00000352397.10:c.684A>T
MANE Select
|
ENSP00000338461.6:p.Lys228Asn
|
|
ENST00000352397.9:c.684A>T
|
ENSP00000338461.6:p.Lys228Asn
|
|
ENST00000361740.8:c.783A>T
|
ENSP00000354468.4:p.Lys261Asn
|
|
ENST00000402438.5:c.615A>T
|
ENSP00000385679.1:p.Lys205Asn
|
|
ENST00000407332.5:c.615A>T
|
ENSP00000384457.1:p.Lys205Asn
|
|
ENST00000407623.7:c.615A>T
|
ENSP00000384834.3:p.Lys205Asn
|
|
ENST00000470741.1:n.2818A>T
|
|
|
NM_000398.6:c.684A>T
|
NP_000389.1:p.Lys228Asn
|
|
NM_001129819.2:c.615A>T
|
NP_001123291.1:p.Lys205Asn
|
|
NM_001171660.1:c.783A>T
|
NP_001165131.1:p.Lys261Asn
|
|
NM_001171661.1:c.615A>T
|
NP_001165132.1:p.Lys205Asn
|
|
NM_007326.4:c.615A>T
|
NP_015565.1:p.Lys205Asn
|
|
NM_000398.7:c.684A>T
MANE Select
|
NP_000389.1:p.Lys228Asn
|
|
NM_001171660.2:c.783A>T
|
NP_001165131.1:p.Lys261Asn
|
|