Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001297764.1 | 2686 | Intron | NP_001284693.1 | ||
NM_005709.3 | 2686 | Intron | NP_005700.2 | ||
NM_153676.3 | 2686 | Missense Mutation | AGA,AGC | R859S | NP_710142.1 |
XM_011519832.2 | 2686 | Intron | XP_011518134.1 | ||
XM_011519834.2 | 2686 | Intron | XP_011518136.1 | ||
XM_017017072.1 | 2686 | Intron | XP_016872561.1 | ||
XM_017017073.1 | 2686 | Intron | XP_016872562.1 | ||
XM_017017074.1 | 2686 | Intron | XP_016872563.1 | ||
XM_017017075.1 | 2686 | Missense Mutation | AGA,AGC | R859S | XP_016872564.1 |