Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_013379.2 | 1402 | Missense Mutation | ATG,GTG | M458V | NP_037511.2 |
XM_005266075.3 | 1402 | Missense Mutation | ATG,GTG | M531V | XP_005266132.1 |
XM_006717083.3 | 1402 | Missense Mutation | CAT,CGT | H508R | XP_006717146.1 |
XM_011518599.2 | 1402 | Missense Mutation | ATG,GTG | M480V | XP_011516901.1 |
XM_011518600.1 | 1402 | Missense Mutation | ATG,GTG | M450V | XP_011516902.1 |
XM_017014651.1 | 1402 | Missense Mutation | CAT,CGT | H457R | XP_016870140.1 |
XM_017014652.1 | 1402 | Missense Mutation | CAT,CGT | H435R | XP_016870141.1 |