Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_013379.2 | 1332 | Silent Mutation | ATC,ATT | I434I | NP_037511.2 |
XM_005266075.3 | 1332 | Silent Mutation | ATC,ATT | I507I | XP_005266132.1 |
XM_006717083.3 | 1332 | Missense Mutation | CGC,TGC | R485C | XP_006717146.1 |
XM_011518599.2 | 1332 | Silent Mutation | ATC,ATT | I456I | XP_011516901.1 |
XM_011518600.1 | 1332 | Silent Mutation | ATC,ATT | I426I | XP_011516902.1 |
XM_017014651.1 | 1332 | Missense Mutation | CGC,TGC | R434C | XP_016870140.1 |
XM_017014652.1 | 1332 | Missense Mutation | CGC,TGC | R412C | XP_016870141.1 |