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Currently, one can select transcripts in the Mutations tab of the Results view, but not anywhere else. Should we consider allowing users to define their default transcripts and propagate them to other places, e.g. oncoprint, patient view?
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Currently, one can select transcripts in the Mutations tab of the Results view, but not anywhere else. Should we consider allowing users to define their default transcripts and propagate them to other places, e.g. oncoprint, patient view?
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