ENST00000326828.6:c.787T>G
MANE Select
|
ENSP00000315602.5:p.Phe263Val
|
|
ENST00000326828.5:c.787T>G
|
ENSP00000315602.5:p.Phe263Val
|
|
ENST00000348639.7:c.787T>G
|
ENSP00000267951.4:p.Phe263Val
|
|
ENST00000558903.1:n.494T>G
|
|
|
ENST00000559658.5:c.787T>G
|
ENSP00000452896.1:p.Phe263Val
|
|
NM_000743.4:c.787T>G
|
NP_000734.2:p.Phe263Val
|
|
NM_001166694.1:c.787T>G
|
NP_001160166.1:p.Phe263Val
|
|
NR_046313.1:n.1288T>G
|
|
|
XM_006720382.1:c.586T>G
|
XP_006720445.1:p.Phe196Val
|
|
XM_011521173.1:c.706T>G
|
XP_011519475.1:p.Phe236Val
|
|
XM_006720382.3:c.586T>G
|
XP_006720445.1:p.Phe196Val
|
|
NM_000743.5:c.787T>G
MANE Select
|
NP_000734.2:p.Phe263Val
|
|
NM_001166694.2:c.787T>G
|
NP_001160166.1:p.Phe263Val
|
|
NR_046313.2:n.989T>G
|
|
|