ENST00000217958.8:c.656T>G
MANE Select
|
ENSP00000217958.3:p.Ile219Arg
|
|
ENST00000217958.7:c.656T>G
|
ENSP00000217958.3:p.Ile219Arg
|
|
ENST00000340200.5:c.557T>G
|
ENSP00000345963.5:p.Ile186Arg
|
|
ENST00000361815.9:c.*121T>G
|
ENSP00000354906.5:n.*121T>G
|
|
ENST00000372295.5:c.533T>G
|
ENSP00000361369.1:p.Ile178Arg
|
|
ENST00000372296.5:c.*121T>G
|
ENSP00000361370.1:n.*121T>G
|
|
NM_002814.3:c.656T>G
|
NP_002805.1:p.Ile219Arg
|
|
NM_170750.2:c.*121T>G
|
NP_736606.1:n.*121T>G
|
|
NM_002814.4:c.656T>G
MANE Select
|
NP_002805.1:p.Ile219Arg
|
|
NM_170750.3:c.*121T>G
|
NP_736606.1:n.*121T>G
|
|