ENST00000350051.8:c.368A>T
MANE Select
|
ENSP00000324180.4:p.Glu123Val
|
|
ENST00000301633.8:c.437A>T
|
ENSP00000301633.3:p.Glu146Val
|
|
ENST00000350051.7:c.368A>T
|
ENSP00000324180.4:p.Glu123Val
|
|
ENST00000374948.6:c.250A>T
|
ENSP00000364086.1:p.Asn84Tyr
|
|
ENST00000589892.1:n.384A>T
|
|
|
ENST00000590925.6:c.*170A>T
|
ENSP00000467336.1:n.*170A>T
|
|
NM_001012270.1:c.250A>T
|
NP_001012270.1:p.Asn84Tyr
|
|
NM_001012271.1:c.437A>T
|
NP_001012271.1:p.Glu146Val
|
|
NM_001168.2:c.368A>T
|
NP_001159.2:p.Glu123Val
|
|
XR_243654.3:n.570A>T
|
|
|
XR_934452.1:n.639A>T
|
|
|
XR_243654.5:n.570A>T
|
|
|
XR_934452.3:n.639A>T
|
|
|
NM_001168.3:c.368A>T
MANE Select
|
NP_001159.2:p.Glu123Val
|
|
NM_001012270.2:c.250A>T
|
NP_001012270.1:p.Asn84Tyr
|
|
NM_001012271.2:c.437A>T
|
NP_001012271.1:p.Glu146Val
|
|