ENST00000217958.8:c.542A>T
MANE Select
|
ENSP00000217958.3:p.Asp181Val
|
|
ENST00000217958.7:c.542A>T
|
ENSP00000217958.3:p.Asp181Val
|
|
ENST00000340200.5:c.443A>T
|
ENSP00000345963.5:p.Asp148Val
|
|
ENST00000361815.9:c.*7A>T
|
ENSP00000354906.5:n.*7A>T
|
|
ENST00000372295.5:c.419A>T
|
ENSP00000361369.1:p.Asp140Val
|
|
ENST00000372296.5:c.*7A>T
|
ENSP00000361370.1:n.*7A>T
|
|
NM_002814.3:c.542A>T
|
NP_002805.1:p.Asp181Val
|
|
NM_170750.2:c.*7A>T
|
NP_736606.1:n.*7A>T
|
|
NM_002814.4:c.542A>T
MANE Select
|
NP_002805.1:p.Asp181Val
|
|
NM_170750.3:c.*7A>T
|
NP_736606.1:n.*7A>T
|
|