Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001130079.2 | 1488 | Missense Mutation | CGC,TGC | R81C | NP_001123551.1 |
NM_001286072.1 | 1488 | Missense Mutation | CGC,TGC | R25C | NP_001273001.1 |
NM_001321324.1 | 1488 | Missense Mutation | CGC,TGC | R81C | NP_001308253.1 |
NM_020963.4 | 1488 | Missense Mutation | CGC,TGC | R81C | NP_066014.1 |
XM_005270869.4 | 1488 | Missense Mutation | CGC,TGC | R25C | XP_005270926.1 |
XM_005270870.4 | 1488 | Missense Mutation | CGC,TGC | R25C | XP_005270927.1 |
XM_017001318.1 | 1488 | Missense Mutation | CGC,TGC | R25C | XP_016856807.1 |
XM_017001319.1 | 1488 | Missense Mutation | CGC,TGC | R81C | XP_016856808.1 |