Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001134432.1 | 913 | Intron | NP_001127904.1 | ||
NM_001134433.1 | 913 | Intron | NP_001127905.1 | ||
NM_001271650.1 | 913 | Missense Mutation | ACA,GCA | T169A | NP_001258579.1 |
NM_022461.4 | 913 | Missense Mutation | ACA,GCA | T281A | NP_071906.1 |
XM_005265392.2 | 913 | Missense Mutation | ACA,GCA | T281A | XP_005265449.1 |
XM_011534009.2 | 913 | Missense Mutation | ACA,GCA | T284A | XP_011532311.1 |
XM_011534010.2 | 913 | Intron | XP_011532312.1 | ||
XM_011534011.2 | 913 | Intron | XP_011532313.1 |