ENST00000350051.8:c.356A>G
MANE Select
|
ENSP00000324180.4:p.Asn119Ser
|
|
ENST00000301633.8:c.425A>G
|
ENSP00000301633.3:p.Asn142Ser
|
|
ENST00000350051.7:c.356A>G
|
ENSP00000324180.4:p.Asn119Ser
|
|
ENST00000374948.6:c.238A>G
|
ENSP00000364086.1:p.Ile80Val
|
|
ENST00000589892.1:n.372A>G
|
|
|
ENST00000590925.6:c.*158A>G
|
ENSP00000467336.1:n.*158A>G
|
|
NM_001012270.1:c.238A>G
|
NP_001012270.1:p.Ile80Val
|
|
NM_001012271.1:c.425A>G
|
NP_001012271.1:p.Asn142Ser
|
|
NM_001168.2:c.356A>G
|
NP_001159.2:p.Asn119Ser
|
|
XR_243654.3:n.558A>G
|
|
|
XR_934452.1:n.627A>G
|
|
|
XR_243654.5:n.558A>G
|
|
|
XR_934452.3:n.627A>G
|
|
|
NM_001168.3:c.356A>G
MANE Select
|
NP_001159.2:p.Asn119Ser
|
|
NM_001012270.2:c.238A>G
|
NP_001012270.1:p.Ile80Val
|
|
NM_001012271.2:c.425A>G
|
NP_001012271.1:p.Asn142Ser
|
|