ENST00000350051.8:c.374A>T
MANE Select
|
ENSP00000324180.4:p.Glu125Val
|
|
ENST00000301633.8:c.443A>T
|
ENSP00000301633.3:p.Glu148Val
|
|
ENST00000350051.7:c.374A>T
|
ENSP00000324180.4:p.Glu125Val
|
|
ENST00000374948.6:c.256A>T
|
ENSP00000364086.1:p.Arg86Trp
|
|
ENST00000589892.1:n.390A>T
|
|
|
ENST00000590925.6:c.*176A>T
|
ENSP00000467336.1:n.*176A>T
|
|
NM_001012270.1:c.256A>T
|
NP_001012270.1:p.Arg86Trp
|
|
NM_001012271.1:c.443A>T
|
NP_001012271.1:p.Glu148Val
|
|
NM_001168.2:c.374A>T
|
NP_001159.2:p.Glu125Val
|
|
XR_243654.3:n.576A>T
|
|
|
XR_934452.1:n.645A>T
|
|
|
XR_243654.5:n.576A>T
|
|
|
XR_934452.3:n.645A>T
|
|
|
NM_001168.3:c.374A>T
MANE Select
|
NP_001159.2:p.Glu125Val
|
|
NM_001012270.2:c.256A>T
|
NP_001012270.1:p.Arg86Trp
|
|
NM_001012271.2:c.443A>T
|
NP_001012271.1:p.Glu148Val
|
|