ENST00000304506.7:c.*1A>G
MANE Select
|
ENSP00000304915.3:n.*1A>G
|
|
ENST00000459878.5:n.446A>G
|
|
|
ENST00000462480.1:n.1513A>G
|
|
|
ENST00000468334.5:n.815A>G
|
|
|
ENST00000487267.5:n.613A>G
|
|
|
ENST00000617259.2:c.397A>G
|
ENSP00000479835.1:p.Asn133Asp
|
|
NM_002188.2:c.*1A>G
|
NP_002179.2:n.*1A>G
|
|
NM_001354991.1:c.*1A>G
|
NP_001341920.1:n.*1A>G
|
|
NM_001354992.1:c.*1A>G
|
NP_001341921.1:n.*1A>G
|
|
NM_001354993.1:c.*1A>G
|
NP_001341922.1:n.*1A>G
|
|
NM_002188.3:c.*1A>G
MANE Select
|
NP_002179.2:n.*1A>G
|
|
NM_001354991.2:c.*1A>G
|
NP_001341920.1:n.*1A>G
|
|
NM_001354992.2:c.*1A>G
|
NP_001341921.1:n.*1A>G
|
|
NM_001354993.2:c.*1A>G
|
NP_001341922.1:n.*1A>G
|
|