ENST00000396659.8:c.407C>T
MANE Select
|
ENSP00000379895.3:p.Thr136Met
|
|
ENST00000674905.1:c.407C>T
|
ENSP00000502176.1:p.Thr136Met
|
|
ENST00000675158.1:c.407C>T
|
ENSP00000501737.1:p.Thr136Met
|
|
ENST00000675323.1:c.407C>T
|
ENSP00000502445.1:p.Thr136Met
|
|
ENST00000675701.1:c.347C>T
|
ENSP00000502671.1:p.Thr116Met
|
|
ENST00000675974.1:n.498C>T
|
|
|
ENST00000676090.1:c.*1138C>T
|
ENSP00000501630.1:n.*1138C>T
|
|
ENST00000396659.7:c.407C>T
|
ENSP00000379895.3:p.Thr136Met
|
|
ENST00000558118.1:c.*212C>T
|
ENSP00000452971.1:n.*212C>T
|
|
ENST00000558163.1:c.188C>T
|
ENSP00000453781.1:p.Thr63Met
|
|
ENST00000558336.5:c.407C>T
|
ENSP00000454008.1:p.Thr136Met
|
|
ENST00000558362.5:n.2063C>T
|
|
|
ENST00000558537.5:c.20C>T
|
ENSP00000453151.1:p.Thr7Met
|
|
ENST00000558916.1:n.305C>T
|
|
|
ENST00000559885.1:c.20C>T
|
ENSP00000453087.1:p.Thr7Met
|
|
ENST00000561148.5:c.20C>T
|
ENSP00000453860.1:p.Thr7Met
|
|
NM_001482.2:c.407C>T
|
NP_001473.1:p.Thr136Met
|
|
XM_011521450.1:c.455C>T
|
XP_011519752.1:p.Thr152Met
|
|
XM_011521451.1:c.449C>T
|
XP_011519753.1:p.Thr150Met
|
|
NM_001321015.1:c.20C>T
|
NP_001307944.1:p.Thr7Met
|
|
NM_001482.3:c.407C>T
MANE Select
|
NP_001473.1:p.Thr136Met
|
|
NM_001321015.2:c.20C>T
|
NP_001307944.1:p.Thr7Met
|
|