ENST00000350051.8:c.399T>C
MANE Select
|
ENSP00000324180.4:p.Arg133=
|
|
ENST00000301633.8:c.468T>C
|
ENSP00000301633.3:p.Arg156=
|
|
ENST00000350051.7:c.399T>C
|
ENSP00000324180.4:p.Arg133=
|
|
ENST00000374948.6:c.281T>C
|
ENSP00000364086.1:p.Val94Ala
|
|
ENST00000589892.1:n.415T>C
|
|
|
ENST00000590925.6:c.*201T>C
|
ENSP00000467336.1:n.*201T>C
|
|
NM_001012270.1:c.281T>C
|
NP_001012270.1:p.Val94Ala
|
|
NM_001012271.1:c.468T>C
|
NP_001012271.1:p.Arg156=
|
|
NM_001168.2:c.399T>C
|
NP_001159.2:p.Arg133=
|
|
XR_243654.3:n.601T>C
|
|
|
XR_934452.1:n.670T>C
|
|
|
XR_243654.5:n.601T>C
|
|
|
XR_934452.3:n.670T>C
|
|
|
NM_001168.3:c.399T>C
MANE Select
|
NP_001159.2:p.Arg133=
|
|
NM_001012270.2:c.281T>C
|
NP_001012270.1:p.Val94Ala
|
|
NM_001012271.2:c.468T>C
|
NP_001012271.1:p.Arg156=
|
|