ENST00000482750.6:c.*37A>T
|
ENSP00000421262.2:n.*37A>T
|
|
ENST00000696903.1:n.1220A>T
|
|
|
ENST00000374202.7:c.917A>T
MANE Select
|
ENSP00000363318.3:p.Asn306Ile
|
|
ENST00000642473.1:n.1281A>T
|
|
|
ENST00000644022.1:n.1183A>T
|
|
|
ENST00000644708.1:n.1226A>T
|
|
|
ENST00000644911.1:n.1323A>T
|
|
|
ENST00000645266.1:c.917A>T
|
ENSP00000493734.1:p.Asn306Ile
|
|
ENST00000645518.1:c.917A>T
|
ENSP00000493986.1:p.Asn306Ile
|
|
ENST00000646106.1:c.917A>T
|
ENSP00000496437.1:p.Asn306Ile
|
|
ENST00000646505.1:c.917A>T
|
ENSP00000496673.1:p.Asn306Ile
|
|
ENST00000647492.1:c.917A>T
|
ENSP00000495340.1:p.Asn306Ile
|
|
ENST00000276110.6:n.1510A>T
|
|
|
ENST00000374188.7:c.104A>T
|
ENSP00000363303.3:p.Asn35Ile
|
|
ENST00000374202.6:c.917A>T
|
ENSP00000363318.2:p.Asn306Ile
|
|
ENST00000456850.6:c.347A>T
|
ENSP00000388967.2:p.Asn116Ile
|
|
ENST00000482750.5:c.233A>T
|
|
|
ENST00000512747.3:n.1096A>T
|
|
|
NM_000206.2:c.917A>T , LRG_150t1:c.917A>T
|
NP_000197.1:p.Asn306Ile
|
|
NM_000206.3:c.917A>T
MANE Select
|
NP_000197.1:p.Asn306Ile
|
|