ENST00000320650.9:c.*341G>T
MANE Select
|
ENSP00000323505.4:n.*341G>T
|
|
ENST00000296545.11:c.*341G>T
|
ENSP00000296545.7:n.*341G>T
|
|
ENST00000320650.8:c.*341G>T
|
ENSP00000323505.4:n.*341G>T
|
|
ENST00000394159.2:c.749G>T
|
ENSP00000377714.1:n.749G>T
|
|
ENST00000477265.5:c.*341G>T
|
ENSP00000436914.1:n.*341G>T
|
|
NM_000585.4:c.*341G>T
|
NP_000576.1:n.*341G>T
|
|
NM_172175.2:c.*341G>T
|
NP_751915.1:n.*341G>T
|
|
NR_037840.2:n.1680G>T
|
|
|
NM_000585.5:c.*341G>T
MANE Select
|
NP_000576.1:n.*341G>T
|
|
NM_172175.3:c.*341G>T
|
NP_751915.1:n.*341G>T
|
|
NR_037840.3:n.1693G>T
|
|
|