ENST00000350051.8:c.*41C>G
MANE Select
|
ENSP00000324180.4:n.*41C>G
|
|
ENST00000301633.8:c.*41C>G
|
ENSP00000301633.3:n.*41C>G
|
|
ENST00000350051.7:c.*41C>G
|
ENSP00000324180.4:n.*41C>G
|
|
ENST00000374948.6:c.352C>G
|
ENSP00000364086.1:p.His118Asp
|
|
ENST00000589892.1:n.486C>G
|
|
|
NM_001012270.1:c.352C>G
|
NP_001012270.1:p.His118Asp
|
|
NM_001012271.1:c.*41C>G
|
NP_001012271.1:n.*41C>G
|
|
NM_001168.2:c.*41C>G
|
NP_001159.2:n.*41C>G
|
|
XR_243654.3:n.672C>G
|
|
|
XR_934452.1:n.741C>G
|
|
|
XR_243654.5:n.672C>G
|
|
|
XR_934452.3:n.741C>G
|
|
|
NM_001168.3:c.*41C>G
MANE Select
|
NP_001159.2:n.*41C>G
|
|
NM_001012270.2:c.352C>G
|
NP_001012270.1:p.His118Asp
|
|
NM_001012271.2:c.*41C>G
|
NP_001012271.1:n.*41C>G
|
|