ENST00000404085.7:c.532G>A
MANE Select
|
ENSP00000384008.3:p.Asp178Asn
|
|
ENST00000404261.9:c.532G>A
|
ENSP00000384753.6:p.Asp178Asn
|
|
ENST00000594072.6:c.532G>A
|
ENSP00000468845.4:p.Asp178Asn
|
|
ENST00000651416.1:n.749G>A
|
|
|
ENST00000652132.1:c.499G>A
|
ENSP00000498416.1:p.Asp167Asn
|
|
ENST00000394458.7:c.694G>A
|
ENSP00000377971.4:p.Asp232Asn
|
|
ENST00000404085.5:c.*431G>A
|
ENSP00000384008.2:n.*431G>A
|
|
ENST00000404261.8:c.694G>A
|
ENSP00000384753.5:p.Asp232Asn
|
|
ENST00000594072.5:c.694G>A
|
ENSP00000468845.3:p.Asp232Asn
|
|
ENST00000596626.1:n.645G>A
|
|
|
ENST00000598347.2:c.534G>A
|
|
|
NM_001278443.1:c.661G>A
|
NP_001265372.1:p.Asp221Asn
|
|
NM_001278444.1:c.694G>A
|
NP_001265373.1:p.Asp232Asn
|
|
NM_001278445.1:c.598G>A
|
NP_001265374.1:p.Asp200Asn
|
|
NM_152363.5:c.694G>A
|
NP_689576.5:p.Asp232Asn
|
|
NR_103530.1:n.808G>A
|
|
|
NM_001278443.2:c.499G>A
|
NP_001265372.2:p.Asp167Asn
|
|
NM_001278444.2:c.532G>A
|
NP_001265373.2:p.Asp178Asn
|
|
NM_001278445.2:c.490G>A
|
NP_001265374.2:p.Asp164Asn
|
|
NM_152363.6:c.532G>A
MANE Select
|
NP_689576.6:p.Asp178Asn
|
|
NR_103530.2:n.552G>A
|
|
|