Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001195790.1 | 7730 | Missense Mutation | CGC,TGC | R327C | NP_001182719.1 |
XM_017024005.1 | 7730 | Missense Mutation | CGC,TGC | R356C | XP_016879494.1 |
XM_017024006.1 | 7730 | Missense Mutation | CGC,TGC | R327C | XP_016879495.1 |
XM_017024007.1 | 7730 | Missense Mutation | CGC,TGC | R327C | XP_016879496.1 |
XM_017024008.1 | 7730 | Missense Mutation | CGC,TGC | R309C | XP_016879497.1 |
XM_017024009.1 | 7730 | Missense Mutation | CGC,TGC | R309C | XP_016879498.1 |