ENST00000217958.8:c.627G>T
MANE Select
|
ENSP00000217958.3:p.Leu209=
|
|
ENST00000217958.7:c.627G>T
|
ENSP00000217958.3:p.Leu209=
|
|
ENST00000340200.5:c.528G>T
|
ENSP00000345963.5:p.Leu176=
|
|
ENST00000361815.9:c.*92G>T
|
ENSP00000354906.5:n.*92G>T
|
|
ENST00000372295.5:c.504G>T
|
ENSP00000361369.1:p.Leu168=
|
|
ENST00000372296.5:c.*92G>T
|
ENSP00000361370.1:n.*92G>T
|
|
NM_002814.3:c.627G>T
|
NP_002805.1:p.Leu209=
|
|
NM_170750.2:c.*92G>T
|
NP_736606.1:n.*92G>T
|
|
NM_002814.4:c.627G>T
MANE Select
|
NP_002805.1:p.Leu209=
|
|
NM_170750.3:c.*92G>T
|
NP_736606.1:n.*92G>T
|
|