ENST00000350051.8:c.411G>A
MANE Select
|
ENSP00000324180.4:p.Gln137=
|
|
ENST00000301633.8:c.480G>A
|
ENSP00000301633.3:p.Gln160=
|
|
ENST00000350051.7:c.411G>A
|
ENSP00000324180.4:p.Gln137=
|
|
ENST00000374948.6:c.293G>A
|
ENSP00000364086.1:p.Ser98Asn
|
|
ENST00000589892.1:n.427G>A
|
|
|
ENST00000590925.6:c.*213G>A
|
ENSP00000467336.1:n.*213G>A
|
|
NM_001012270.1:c.293G>A
|
NP_001012270.1:p.Ser98Asn
|
|
NM_001012271.1:c.480G>A
|
NP_001012271.1:p.Gln160=
|
|
NM_001168.2:c.411G>A
|
NP_001159.2:p.Gln137=
|
|
XR_243654.3:n.613G>A
|
|
|
XR_934452.1:n.682G>A
|
|
|
XR_243654.5:n.613G>A
|
|
|
XR_934452.3:n.682G>A
|
|
|
NM_001168.3:c.411G>A
MANE Select
|
NP_001159.2:p.Gln137=
|
|
NM_001012270.2:c.293G>A
|
NP_001012270.1:p.Ser98Asn
|
|
NM_001012271.2:c.480G>A
|
NP_001012271.1:p.Gln160=
|
|