ENST00000482750.6:c.*38C>A
|
ENSP00000421262.2:n.*38C>A
|
|
ENST00000696903.1:n.1221C>A
|
|
|
ENST00000374202.7:c.918C>A
MANE Select
|
ENSP00000363318.3:p.Asn306Lys
|
|
ENST00000642473.1:n.1282C>A
|
|
|
ENST00000644022.1:n.1184C>A
|
|
|
ENST00000644708.1:n.1227C>A
|
|
|
ENST00000644911.1:n.1324C>A
|
|
|
ENST00000645266.1:c.918C>A
|
ENSP00000493734.1:p.Asn306Lys
|
|
ENST00000645518.1:c.918C>A
|
ENSP00000493986.1:p.Asn306Lys
|
|
ENST00000646106.1:c.918C>A
|
ENSP00000496437.1:p.Asn306Lys
|
|
ENST00000646505.1:c.918C>A
|
ENSP00000496673.1:p.Asn306Lys
|
|
ENST00000647492.1:c.918C>A
|
ENSP00000495340.1:p.Asn306Lys
|
|
ENST00000276110.6:n.1511C>A
|
|
|
ENST00000374188.7:c.105C>A
|
ENSP00000363303.3:p.Asn35Lys
|
|
ENST00000374202.6:c.918C>A
|
ENSP00000363318.2:p.Asn306Lys
|
|
ENST00000456850.6:c.348C>A
|
ENSP00000388967.2:p.Asn116Lys
|
|
ENST00000482750.5:c.234C>A
|
|
|
ENST00000512747.3:n.1097C>A
|
|
|
NM_000206.2:c.918C>A , LRG_150t1:c.918C>A
|
NP_000197.1:p.Asn306Lys
|
|
NM_000206.3:c.918C>A
MANE Select
|
NP_000197.1:p.Asn306Lys
|
|