|
ENST00000396659.8:c.1237C>T
MANE Select
|
ENSP00000379895.3:p.Arg413Trp
|
|
|
ENST00000674905.1:c.*199C>T
|
ENSP00000502176.1:n.*199C>T
|
|
|
ENST00000675158.1:c.*137C>T
|
ENSP00000501737.1:n.*137C>T
|
|
|
ENST00000675323.1:c.*1739C>T
|
ENSP00000502445.1:n.*1739C>T
|
|
|
ENST00000675701.1:c.1177C>T
|
ENSP00000502671.1:p.Arg393Trp
|
|
|
ENST00000675974.1:n.3786C>T
|
|
|
|
ENST00000676090.1:c.*1968C>T
|
ENSP00000501630.1:n.*1968C>T
|
|
|
ENST00000396659.7:c.1237C>T
|
ENSP00000379895.3:p.Arg413Trp
|
|
|
ENST00000558362.5:n.2893C>T
|
|
|
|
NM_001482.2:c.1237C>T
|
NP_001473.1:p.Arg413Trp
|
|
|
XM_011521450.1:c.1285C>T
|
XP_011519752.1:p.Arg429Trp
|
|
|
XM_011521451.1:c.1279C>T
|
XP_011519753.1:p.Arg427Trp
|
|
|
NM_001321015.1:c.850C>T
|
NP_001307944.1:p.Arg284Trp
|
|
|
NM_001482.3:c.1237C>T
MANE Select
|
NP_001473.1:p.Arg413Trp
|
|
|
NM_001321015.2:c.850C>T
|
NP_001307944.1:p.Arg284Trp
|
|
