Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_175078.2 | 1248 | Missense Mutation | AAC,AGC | N486S | NP_778253.2 |
XM_011538288.2 | 1248 | Missense Mutation | AAC,AGC | N253S | XP_011536590.1 |
XM_011538289.2 | 1248 | Intron | XP_011536591.1 |