Not from UniProt because I don't think the isoforms are run through Pfam. Running each of them them yourself would be hard work and I'm not sure how useful that would be. Isoforms with a missing exon (i.e. most of them) would just gap the global allignments that are compiled from the canonical (all exon) forms
If you could expand on the biological question you are trying to answer I might be able to help more. On a a coordinates basis sure - you can map domain markup across to residue positions in isoforms but this is not biologically valid. If you delete a sizable exon chunk out of a Pfam domain (or any other InterPro signature in fact) that part of the protein is probably not going to fold properly - regardless of domain boundaries.
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Ram
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cdsouthan
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So what would you do if you'd like to map the domains from the canonical transcript to the isoforms?
If you could expand on the biological question you are trying to answer I might be able to help more. On a a coordinates basis sure - you can map domain markup across to residue positions in isoforms but this is not biologically valid. If you delete a sizable exon chunk out of a Pfam domain (or any other InterPro signature in fact) that part of the protein is probably not going to fold properly - regardless of domain boundaries.