Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015567.1 | 972 | Missense Mutation | CTT,TTT | L28F | NP_056382.1 |
XM_005254038.4 | 972 | Missense Mutation | CTT,TTT | L28F | XP_005254095.1 |
XM_005254039.2 | 972 | Missense Mutation | CTT,TTT | L28F | XP_005254096.1 |