ENST00000359478.7:c.463A>T
MANE Select
|
ENSP00000352455.2:p.Asn155Tyr
|
|
ENST00000359478.6:c.463A>T
|
ENSP00000352455.2:p.Asn155Tyr
|
|
ENST00000396549.6:c.433A>T
|
ENSP00000379798.2:p.Asn145Tyr
|
|
ENST00000433590.6:c.388A>T
|
ENSP00000411997.2:p.Asn130Tyr
|
|
ENST00000535336.5:c.271A>T
|
ENSP00000438525.1:p.Asn91Tyr
|
|
ENST00000535411.5:c.432A>T
|
|
|
ENST00000537009.5:c.*115A>T
|
ENSP00000439289.1:n.*115A>T
|
|
ENST00000538694.5:n.422A>T
|
|
|
ENST00000540087.5:c.433A>T
|
ENSP00000440496.1:p.Asn145Tyr
|
|
ENST00000543369.5:c.397A>T
|
ENSP00000441492.1:p.Asn133Tyr
|
|
ENST00000543467.5:c.181A>T
|
ENSP00000444531.1:p.Asn61Tyr
|
|
ENST00000544211.5:c.*115A>T
|
ENSP00000443839.1:n.*115A>T
|
|
NM_001297709.1:c.433A>T
|
NP_001284638.1:p.Asn145Tyr
|
|
NM_001297710.1:c.397A>T
|
NP_001284639.1:p.Asn133Tyr
|
|
NM_001297711.1:c.388A>T
|
NP_001284640.1:p.Asn130Tyr
|
|
NM_001297712.1:c.271A>T
|
NP_001284641.1:p.Asn91Tyr
|
|
NM_003480.3:c.463A>T
|
NP_003471.1:p.Asn155Tyr
|
|
NR_123733.1:n.796A>T
|
|
|
NR_123734.1:n.766A>T
|
|
|
NM_003480.4:c.463A>T
MANE Select
|
NP_003471.1:p.Asn155Tyr
|
|
NM_001297709.2:c.433A>T
|
NP_001284638.1:p.Asn145Tyr
|
|
NM_001297710.2:c.397A>T
|
NP_001284639.1:p.Asn133Tyr
|
|
NM_001297711.2:c.388A>T
|
NP_001284640.1:p.Asn130Tyr
|
|
NM_001297712.2:c.271A>T
|
NP_001284641.1:p.Asn91Tyr
|
|
NR_123733.2:n.734A>T
|
|
|
NR_123734.2:n.704A>T
|
|
|