Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_213604.2 | 1674 | Missense Mutation | CCT,CTT | P456L | NP_998769.2 |
XM_005259549.3 | 1674 | Missense Mutation | CCT,CTT | P466L | XP_005259606.1 |
XM_011527961.1 | 1674 | Missense Mutation | CCT,CTT | P470L | XP_011526263.1 |
XM_011527963.1 | 1674 | Missense Mutation | CCT,CTT | P225L | XP_011526265.1 |
XM_017026744.1 | 1674 | Missense Mutation | CCT,CTT | P460L | XP_016882233.1 |
XM_017026745.1 | 1674 | Missense Mutation | CCT,CTT | P456L | XP_016882234.1 |