ENST00000350051.8:c.355A>G
MANE Select
|
ENSP00000324180.4:p.Asn119Asp
|
|
ENST00000301633.8:c.424A>G
|
ENSP00000301633.3:p.Asn142Asp
|
|
ENST00000350051.7:c.355A>G
|
ENSP00000324180.4:p.Asn119Asp
|
|
ENST00000374948.6:c.237A>G
|
ENSP00000364086.1:p.Thr79=
|
|
ENST00000589892.1:n.371A>G
|
|
|
ENST00000590925.6:c.*157A>G
|
ENSP00000467336.1:n.*157A>G
|
|
NM_001012270.1:c.237A>G
|
NP_001012270.1:p.Thr79=
|
|
NM_001012271.1:c.424A>G
|
NP_001012271.1:p.Asn142Asp
|
|
NM_001168.2:c.355A>G
|
NP_001159.2:p.Asn119Asp
|
|
XR_243654.3:n.557A>G
|
|
|
XR_934452.1:n.626A>G
|
|
|
XR_243654.5:n.557A>G
|
|
|
XR_934452.3:n.626A>G
|
|
|
NM_001168.3:c.355A>G
MANE Select
|
NP_001159.2:p.Asn119Asp
|
|
NM_001012270.2:c.237A>G
|
NP_001012270.1:p.Thr79=
|
|
NM_001012271.2:c.424A>G
|
NP_001012271.1:p.Asn142Asp
|
|