Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001980.3 | 1159 | Silent Mutation | TCA,TCC | S287S | NP_001971.2 |
NM_194356.2 | 1159 | UTR 3 | NP_919337.1 | ||
XM_005253557.1 | 1159 | Missense Mutation | CAT,CCT | H267P | XP_005253614.1 |
XM_017018978.1 | 1159 | UTR 3 | XP_016874467.1 | ||
XM_017018979.1 | 1159 | UTR 3 | XP_016874468.1 | ||
XM_017018980.1 | 1159 | Silent Mutation | TCA,TCC | S319S | XP_016874469.1 |
XM_017018981.1 | 1159 | Intron | XP_016874470.1 | ||
XM_017018982.1 | 1159 | Missense Mutation | CAT,CCT | H299P | XP_016874471.1 |
XM_017018983.1 | 1159 | UTR 3 | XP_016874472.1 | ||
XM_017018984.1 | 1159 | UTR 3 | XP_016874473.1 | ||
XM_017018985.1 | 1159 | Silent Mutation | TCA,TCC | S213S | XP_016874474.1 |
XM_017018986.1 | 1159 | Intron | XP_016874475.1 | ||
XM_017018987.1 | 1159 | Intron | XP_016874476.1 | ||
XM_017018988.1 | 1159 | Intron | XP_016874477.1 | ||
XM_017018989.1 | 1159 | Intron | XP_016874478.1 |