Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_002558.3 | 1627 | Missense Mutation | ATG,GTG | M396V | NP_002549.1 |
XM_006721529.2 | 1627 | Missense Mutation | ATG,GTG | M379V | XP_006721592.1 |
XM_011523896.2 | 1627 | Missense Mutation | ATG,GTG | M428V | XP_011522198.1 |
XM_011523897.2 | 1627 | Missense Mutation | ATG,GTG | M416V | XP_011522199.1 |
XM_011523898.2 | 1627 | Missense Mutation | ATG,GTG | M411V | XP_011522200.1 |
XM_011523899.2 | 1627 | Missense Mutation | ATG,GTG | M408V | XP_011522201.1 |
XM_011523900.2 | 1627 | Intron | XP_011522202.1 |