Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015540.3 | 4511 | Missense Mutation | CAC,CTC | H1366L | NP_056355.2 |
XM_005254297.1 | 4511 | Missense Mutation | CAC,CTC | H1366L | XP_005254354.1 |
XM_006720469.1 | 4511 | Missense Mutation | CAC,CTC | H1306L | XP_006720532.1 |