Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001001325.2 | 597 | Intron | NP_001001325.1 | ||
XM_017009466.1 | 597 | Intron | XP_016864955.1 | ||
XM_017009467.1 | 597 | Silent Mutation | CTC,CTT | L66L | XP_016864956.1 |
XM_017009468.1 | 597 | UTR 5 | XP_016864957.1 | ||
XM_017009469.1 | 597 | Intron | XP_016864958.1 |