Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001270998.1 | 502 | Missense Mutation | AAC,ACC | N141T | NP_001257927.1 |
NM_001270999.1 | 502 | Missense Mutation | AAC,ACC | N97T | NP_001257928.1 |
NM_138802.2 | 502 | Missense Mutation | AAC,ACC | N141T | NP_620157.1 |
XM_006712285.1 | 502 | Missense Mutation | AAC,ACC | N141T | XP_006712348.1 |
XM_006712286.3 | 502 | Missense Mutation | AAC,ACC | N141T | XP_006712349.1 |
XM_017003368.1 | 502 | Missense Mutation | AAC,ACC | N141T | XP_016858857.1 |