ENST00000217958.8:c.592A>G
MANE Select
|
ENSP00000217958.3:p.Ile198Val
|
|
ENST00000217958.7:c.592A>G
|
ENSP00000217958.3:p.Ile198Val
|
|
ENST00000340200.5:c.493A>G
|
ENSP00000345963.5:p.Ile165Val
|
|
ENST00000361815.9:c.*57A>G
|
ENSP00000354906.5:n.*57A>G
|
|
ENST00000372295.5:c.469A>G
|
ENSP00000361369.1:p.Ile157Val
|
|
ENST00000372296.5:c.*57A>G
|
ENSP00000361370.1:n.*57A>G
|
|
NM_002814.3:c.592A>G
|
NP_002805.1:p.Ile198Val
|
|
NM_170750.2:c.*57A>G
|
NP_736606.1:n.*57A>G
|
|
NM_002814.4:c.592A>G
MANE Select
|
NP_002805.1:p.Ile198Val
|
|
NM_170750.3:c.*57A>G
|
NP_736606.1:n.*57A>G
|
|