ENST00000355943.8:c.1250A>T
MANE Select
|
ENSP00000348211.3:p.Asn417Ile
|
|
ENST00000355943.7:c.1250A>T
|
ENSP00000348211.3:p.Asn417Ile
|
|
ENST00000447245.6:c.1007A>T
|
ENSP00000399717.2:p.Asn336Ile
|
|
ENST00000504098.1:c.812A>T
|
ENSP00000425708.1:p.Asn271Ile
|
|
ENST00000509432.1:c.611A>T
|
ENSP00000426604.1:p.Asn204Ile
|
|
ENST00000513706.2:n.2850A>T
|
|
|
ENST00000513807.5:c.764A>T
|
ENSP00000421134.1:p.Asn255Ile
|
|
NM_001303249.1:c.1007A>T
|
NP_001290178.1:p.Asn336Ile
|
|
NM_001303250.1:c.977A>T
|
NP_001290179.1:p.Asn326Ile
|
|
NM_138773.2:c.1250A>T
|
NP_620128.1:p.Asn417Ile
|
|
NM_001303249.2:c.1007A>T
|
NP_001290178.1:p.Asn336Ile
|
|
NM_001303250.2:c.977A>T
|
NP_001290179.1:p.Asn326Ile
|
|
NM_138773.3:c.1250A>T
|
NP_620128.1:p.Asn417Ile
|
|
NR_138151.1:n.1524A>T
|
|
|
NM_138773.4:c.1250A>T
MANE Select
|
NP_620128.1:p.Asn417Ile
|
|
NM_001303249.3:c.1007A>T
|
NP_001290178.1:p.Asn336Ile
|
|
NM_001303250.3:c.977A>T
|
NP_001290179.1:p.Asn326Ile
|
|
NR_138151.2:n.1489A>T
|
|
|