Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001199295.1 | 617 | Missense Mutation | CCT,CGT | P98R | NP_001186224.1 |
NM_153263.2 | 617 | Missense Mutation | CCT,CGT | P85R | NP_694995.2 |
XM_006723128.3 | 617 | Missense Mutation | CCT,CGT | P76R | XP_006723191.1 |