ENST00000258385.8:c.1328A>T
MANE Select
|
ENSP00000258385.3:p.Asn443Ile
|
|
ENST00000258385.7:c.1328A>T
|
ENSP00000258385.3:p.Asn443Ile
|
|
ENST00000441621.6:c.*510A>T
|
ENSP00000408819.2:n.*510A>T
|
|
ENST00000446616.1:c.*969A>T
|
ENSP00000410801.1:n.*969A>T
|
|
ENST00000543200.5:c.1283A>T
|
ENSP00000438380.1:p.Asn428Ile
|
|
NM_000751.2:c.1328A>T
|
NP_000742.1:p.Asn443Ile
|
|
NM_001256657.1:c.1283A>T
|
NP_001243586.1:p.Asn428Ile
|
|
NM_001311195.1:c.746A>T
|
NP_001298124.1:p.Asn249Ile
|
|
NM_001311196.1:c.1025A>T
|
NP_001298125.1:p.Asn342Ile
|
|
NR_046333.1:c.-4294966223A>T
|
|
|
NR_046334.1:c.-4294965944A>T
|
|
|
XM_011510524.1:c.947A>T
|
XP_011508826.1:p.Asn316Ile
|
|
XM_011510524.2:c.947A>T
|
XP_011508826.1:p.Asn316Ile
|
|
NM_000751.3:c.1328A>T
MANE Select
|
NP_000742.1:p.Asn443Ile
|
|
NM_001311195.2:c.746A>T
|
NP_001298124.1:p.Asn249Ile
|
|
NM_001311196.2:c.1025A>T
|
NP_001298125.1:p.Asn342Ile
|
|
NM_001256657.2:c.1283A>T
|
NP_001243586.1:p.Asn428Ile
|
|