Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_000603.4 | 399 | Missense Mutation | AGC,GGC | S116G | NP_000594.2 |
NM_001160109.1 | 399 | Missense Mutation | AGC,GGC | S116G | NP_001153581.1 |
NM_001160110.1 | 399 | Missense Mutation | AGC,GGC | S116G | NP_001153582.1 |
NM_001160111.1 | 399 | Missense Mutation | AGC,GGC | S116G | NP_001153583.1 |
XM_006716002.3 | 399 | Missense Mutation | AGC,GGC | S116G | XP_006716065.1 |
XM_017012232.1 | 399 | Missense Mutation | AGC,GGC | S116G | XP_016867721.1 |
XM_017012233.1 | 399 | UTR 5 | XP_016867722.1 | ||
XM_017012234.1 | 399 | Missense Mutation | AGC,GGC | S116G | XP_016867723.1 |