ENST00000587656.6:c.6035T>G
|
ENSP00000468638.2:p.Phe2012Cys
|
|
ENST00000294618.12:c.5930T>G
MANE Select
|
ENSP00000294618.6:p.Phe1977Cys
|
|
ENST00000294618.11:c.5930T>G
|
ENSP00000294618.6:p.Phe1977Cys
|
|
ENST00000586702.1:n.833T>G
|
|
|
ENST00000587656.5:c.3795T>G
|
|
|
ENST00000587734.1:c.75+1164T>G
|
ENSP00000468291.1:n.75+1164T>G
|
|
NM_020812.3:c.5930T>G
|
NP_065863.2:p.Phe1977Cys
|
|
XM_005260000.2:c.6128T>G
|
XP_005260057.1:p.Phe2043Cys
|
|
XM_005260001.2:c.6035T>G
|
XP_005260058.1:p.Phe2012Cys
|
|
XM_006722804.2:c.3266T>G
|
XP_006722867.1:p.Phe1089Cys
|
|
XM_011528150.1:c.6068T>G
|
XP_011526452.1:p.Phe2023Cys
|
|
XM_011528151.1:c.6056T>G
|
XP_011526453.1:p.Phe2019Cys
|
|
XM_011528152.1:c.5963T>G
|
XP_011526454.1:p.Phe1988Cys
|
|
XR_936195.1:n.6175T>G
|
|
|
XM_006722804.3:c.3266T>G
|
XP_006722867.1:p.Phe1089Cys
|
|
NM_001367830.1:c.6035T>G
|
NP_001354759.1:p.Phe2012Cys
|
|
NM_020812.4:c.5930T>G
MANE Select
|
NP_065863.2:p.Phe1977Cys
|
|