ENST00000350051.8:c.376G>C
MANE Select
|
ENSP00000324180.4:p.Glu126Gln
|
|
ENST00000301633.8:c.445G>C
|
ENSP00000301633.3:p.Glu149Gln
|
|
ENST00000350051.7:c.376G>C
|
ENSP00000324180.4:p.Glu126Gln
|
|
ENST00000374948.6:c.258G>C
|
ENSP00000364086.1:p.Arg86Ser
|
|
ENST00000589892.1:n.392G>C
|
|
|
ENST00000590925.6:c.*178G>C
|
ENSP00000467336.1:n.*178G>C
|
|
NM_001012270.1:c.258G>C
|
NP_001012270.1:p.Arg86Ser
|
|
NM_001012271.1:c.445G>C
|
NP_001012271.1:p.Glu149Gln
|
|
NM_001168.2:c.376G>C
|
NP_001159.2:p.Glu126Gln
|
|
XR_243654.3:n.578G>C
|
|
|
XR_934452.1:n.647G>C
|
|
|
XR_243654.5:n.578G>C
|
|
|
XR_934452.3:n.647G>C
|
|
|
NM_001168.3:c.376G>C
MANE Select
|
NP_001159.2:p.Glu126Gln
|
|
NM_001012270.2:c.258G>C
|
NP_001012270.1:p.Arg86Ser
|
|
NM_001012271.2:c.445G>C
|
NP_001012271.1:p.Glu149Gln
|
|