ENST00000304506.7:c.436A>C
MANE Select
|
ENSP00000304915.3:p.Asn146His
|
|
ENST00000459878.5:n.440A>C
|
|
|
ENST00000462480.1:n.1507A>C
|
|
|
ENST00000468334.5:n.809A>C
|
|
|
ENST00000487267.5:n.607A>C
|
|
|
ENST00000617259.2:c.394A>C
|
ENSP00000479835.1:p.Asn132His
|
|
NM_002188.2:c.436A>C
|
NP_002179.2:p.Asn146His
|
|
NM_001354991.1:c.241A>C
|
NP_001341920.1:p.Asn81His
|
|
NM_001354992.1:c.241A>C
|
NP_001341921.1:p.Asn81His
|
|
NM_001354993.1:c.241A>C
|
NP_001341922.1:p.Asn81His
|
|
NM_002188.3:c.436A>C
MANE Select
|
NP_002179.2:p.Asn146His
|
|
NM_001354991.2:c.241A>C
|
NP_001341920.1:p.Asn81His
|
|
NM_001354992.2:c.241A>C
|
NP_001341921.1:p.Asn81His
|
|
NM_001354993.2:c.241A>C
|
NP_001341922.1:p.Asn81His
|
|