Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001272038.1 | 813 | Missense Mutation | CCC,CGC | P104R | NP_001258967.1 |
NM_002870.3 | 813 | Missense Mutation | CCC,CGC | P185R | NP_002861.1 |
XM_017001959.1 | 813 | Intron | XP_016857448.1 |