Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_003196.2 | 1542 | Intron | NP_003187.1 | ||
XM_006710864.1 | 1542 | UTR 3 | XP_006710927.1 | ||
XM_011542053.2 | 1542 | Intron | XP_011540355.1 | ||
XM_017002200.1 | 1542 | Missense Mutation | ACG,ATG | T484M | XP_016857689.1 |
XM_017002201.1 | 1542 | Missense Mutation | ACG,ATG | T463M | XP_016857690.1 |
XM_017002202.1 | 1542 | Missense Mutation | ACG,ATG | T463M | XP_016857691.1 |
XM_017002203.1 | 1542 | Missense Mutation | ACG,ATG | T447M | XP_016857692.1 |
XM_017002204.1 | 1542 | Intron | XP_016857693.1 |