Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_015721.2 | 3182 | Missense Mutation | CGC,TGC | R949C | NP_056536.2 |
XM_005256667.4 | 3182 | Missense Mutation | CGC,TGC | R953C | XP_005256724.1 |
XM_005256670.4 | 3182 | Missense Mutation | CGC,TGC | R938C | XP_005256727.1 |
XM_011523910.2 | 3182 | Missense Mutation | CGC,TGC | R953C | XP_011522212.1 |
XM_011523911.2 | 3182 | Missense Mutation | CGC,TGC | R953C | XP_011522213.1 |
XM_011523912.2 | 3182 | Missense Mutation | CGC,TGC | R938C | XP_011522214.1 |
XM_011523913.2 | 3182 | Missense Mutation | CGC,TGC | R938C | XP_011522215.1 |
XM_017024709.1 | 3182 | Missense Mutation | CGC,TGC | R953C | XP_016880198.1 |