Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001267033.1 | 3065 | UTR 3 | NP_001253962.1 | ||
NM_003422.2 | 3065 | Missense Mutation | CGC,GGC | R717G | NP_003413.2 |
NM_198055.1 | 3065 | Missense Mutation | CGC,GGC | R717G | NP_932172.1 |
XM_005259204.3 | 3065 | Missense Mutation | CGC,GGC | R758G | XP_005259261.1 |
XM_011527264.2 | 3065 | Missense Mutation | CGC,GGC | R747G | XP_011525566.1 |
XM_017027206.1 | 3065 | Missense Mutation | CGC,GGC | R433G | XP_016882695.1 |