ENST00000350051.8:c.377A>G
MANE Select
|
ENSP00000324180.4:p.Glu126Gly
|
|
ENST00000301633.8:c.446A>G
|
ENSP00000301633.3:p.Glu149Gly
|
|
ENST00000350051.7:c.377A>G
|
ENSP00000324180.4:p.Glu126Gly
|
|
ENST00000374948.6:c.259A>G
|
ENSP00000364086.1:p.Lys87Glu
|
|
ENST00000589892.1:n.393A>G
|
|
|
ENST00000590925.6:c.*179A>G
|
ENSP00000467336.1:n.*179A>G
|
|
NM_001012270.1:c.259A>G
|
NP_001012270.1:p.Lys87Glu
|
|
NM_001012271.1:c.446A>G
|
NP_001012271.1:p.Glu149Gly
|
|
NM_001168.2:c.377A>G
|
NP_001159.2:p.Glu126Gly
|
|
XR_243654.3:n.579A>G
|
|
|
XR_934452.1:n.648A>G
|
|
|
XR_243654.5:n.579A>G
|
|
|
XR_934452.3:n.648A>G
|
|
|
NM_001168.3:c.377A>G
MANE Select
|
NP_001159.2:p.Glu126Gly
|
|
NM_001012270.2:c.259A>G
|
NP_001012270.1:p.Lys87Glu
|
|
NM_001012271.2:c.446A>G
|
NP_001012271.1:p.Glu149Gly
|
|