ENST00000350051.8:c.385G=
MANE Select
|
ENSP00000324180.4:p.Glu129=
|
|
ENST00000301633.8:c.454G=
|
ENSP00000301633.3:p.Glu152=
|
|
ENST00000350051.7:c.385G=
|
ENSP00000324180.4:p.Glu129=
|
|
ENST00000374948.6:c.267G=
|
ENSP00000364086.1:p.Arg89=
|
|
ENST00000589892.1:n.401G=
|
|
|
ENST00000590925.6:c.*187G=
|
ENSP00000467336.1:n.*187G=
|
|
NM_001012270.1:c.267G=
|
NP_001012270.1:p.Arg89=
|
|
NM_001012271.1:c.454G=
|
NP_001012271.1:p.Glu152=
|
|
NM_001168.2:c.385G=
|
NP_001159.2:p.Glu129=
|
|
XR_243654.3:n.587G=
|
|
|
XR_934452.1:n.656G=
|
|
|
XR_243654.5:n.587G=
|
|
|
XR_934452.3:n.656G=
|
|
|
NM_001168.3:c.385G=
MANE Select
|
NP_001159.2:p.Glu129=
|
|
NM_001012270.2:c.267G=
|
NP_001012270.1:p.Arg89=
|
|
NM_001012271.2:c.454G=
|
NP_001012271.1:p.Glu152=
|
|