ENST00000258385.8:c.1352A>T
MANE Select
|
ENSP00000258385.3:p.Asp451Val
|
|
ENST00000258385.7:c.1352A>T
|
ENSP00000258385.3:p.Asp451Val
|
|
ENST00000441621.6:c.*534A>T
|
ENSP00000408819.2:n.*534A>T
|
|
ENST00000446616.1:c.*993A>T
|
ENSP00000410801.1:n.*993A>T
|
|
ENST00000543200.5:c.1307A>T
|
ENSP00000438380.1:p.Asp436Val
|
|
NM_000751.2:c.1352A>T
|
NP_000742.1:p.Asp451Val
|
|
NM_001256657.1:c.1307A>T
|
NP_001243586.1:p.Asp436Val
|
|
NM_001311195.1:c.770A>T
|
NP_001298124.1:p.Asp257Val
|
|
NM_001311196.1:c.1049A>T
|
NP_001298125.1:p.Asp350Val
|
|
NR_046333.1:c.-4294966199A>T
|
|
|
NR_046334.1:c.-4294965920A>T
|
|
|
XM_011510524.1:c.971A>T
|
XP_011508826.1:p.Asp324Val
|
|
XM_011510524.2:c.971A>T
|
XP_011508826.1:p.Asp324Val
|
|
NM_000751.3:c.1352A>T
MANE Select
|
NP_000742.1:p.Asp451Val
|
|
NM_001311195.2:c.770A>T
|
NP_001298124.1:p.Asp257Val
|
|
NM_001311196.2:c.1049A>T
|
NP_001298125.1:p.Asp350Val
|
|
NM_001256657.2:c.1307A>T
|
NP_001243586.1:p.Asp436Val
|
|