Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001130143.1 | 608 | Missense Mutation | ATC,CTC | I182L | NP_001123615.1 |
NM_017726.7 | 608 | Missense Mutation | CAT,CCT | H143P | NP_060196.1 |
XM_017022372.1 | 608 | UTR 3 | XP_016877861.1 |