Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001004309.2 | 239 | Missense Mutation | AAT,AGT | N18S | NP_001004309.2 |
XM_017022127.1 | 239 | UTR 5 | XP_016877616.1 | ||
XM_017022128.1 | 239 | Intron | XP_016877617.1 | ||
XM_017022129.1 | 239 | UTR 5 | XP_016877618.1 |