ENST00000696133.1:c.1283T>A
|
ENSP00000512426.1:p.Ile428Asn
|
|
ENST00000696134.1:c.*710T>A
|
ENSP00000512427.1:n.*710T>A
|
|
ENST00000367021.8:c.1283T>A
MANE Select
|
ENSP00000355988.3:p.Ile428Asn
|
|
ENST00000643798.1:c.*793T>A
|
ENSP00000496669.1:n.*793T>A
|
|
ENST00000367021.7:c.1283T>A
|
ENSP00000355988.3:p.Ile428Asn
|
|
ENST00000542854.5:c.998T>A
|
ENSP00000440532.1:p.Ile333Asn
|
|
NM_001206696.1:c.998T>A
|
NP_001193625.1:p.Ile333Asn
|
|
NM_006147.3:c.1283T>A
|
NP_006138.1:p.Ile428Asn
|
|
NM_006147.4:c.1283T>A
MANE Select
|
NP_006138.1:p.Ile428Asn
|
|
NM_001206696.2:c.998T>A
|
NP_001193625.1:p.Ile333Asn
|
|