Hi everyone, I am pretty new in bioinformatics and I am struggling to convert the ensembl transcript ID I got from my salmon quant.sf into symbol. The problem is that when I run the script below, I get more rows than my query, so I can't align my annotations in my results table. I hope I was clear enough. If you could give me a hit would be highly appreciated :)

library(biomaRt)
    listMarts()
    ensembl=useMart("ENSEMBL_MART_ENSEMBL")
    listDatasets(ensembl) 
    ensembl <- useDataset("mmusculus_gene_ensembl", mart = ensembl)

    listAttributes(ensembl)

    filterType <- "ensembl_transcript_id_version"
    filterValues <- rownames(res4)        #this are my results from Deseq2

    attributeNames <- c('ensembl_transcript_id_version', 'entrezgene_id', 'mgi_symbol')

    annot <- getBM(attributes=attributeNames, 
                   filters = filterType, 
                   values = filterValues, 
                   mart = ensemble)

length(rownames(res4))

[1] 58400

annot

58655

I know that it is normal to get more transcripts per gene, but how I can align then my results? Thanks in advance :)