ENST00000326828.6:c.437A>T
MANE Select
|
ENSP00000315602.5:p.Glu146Val
|
|
ENST00000326828.5:c.437A>T
|
ENSP00000315602.5:p.Glu146Val
|
|
ENST00000348639.7:c.437A>T
|
ENSP00000267951.4:p.Glu146Val
|
|
ENST00000558903.1:n.144A>T
|
|
|
ENST00000559658.5:c.437A>T
|
ENSP00000452896.1:p.Glu146Val
|
|
NM_000743.4:c.437A>T
|
NP_000734.2:p.Glu146Val
|
|
NM_001166694.1:c.437A>T
|
NP_001160166.1:p.Glu146Val
|
|
NR_046313.1:n.938A>T
|
|
|
XM_006720382.1:c.236A>T
|
XP_006720445.1:p.Glu79Val
|
|
XM_011521173.1:c.356A>T
|
XP_011519475.1:p.Glu119Val
|
|
XM_006720382.3:c.236A>T
|
XP_006720445.1:p.Glu79Val
|
|
NM_000743.5:c.437A>T
MANE Select
|
NP_000734.2:p.Glu146Val
|
|
NM_001166694.2:c.437A>T
|
NP_001160166.1:p.Glu146Val
|
|
NR_046313.2:n.639A>T
|
|
|