Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001308207.1 | 3159 | Missense Mutation | CCT,TCT | P934S | NP_001295136.1 |
NM_001308208.1 | 3159 | Missense Mutation | CCT,TCT | P934S | NP_001295137.1 |
NM_025251.2 | 3159 | Missense Mutation | CCT,TCT | P965S | NP_079527.1 |
XM_011517308.1 | 3159 | Missense Mutation | CCT,TCT | P965S | XP_011515610.1 |
XM_011517309.1 | 3159 | Missense Mutation | CCT,TCT | P965S | XP_011515611.1 |
XM_011517312.2 | 3159 | Missense Mutation | CCT,TCT | P808S | XP_011515614.1 |
XM_017013870.1 | 3159 | Missense Mutation | CCT,TCT | P965S | XP_016869359.1 |
XM_017013871.1 | 3159 | Missense Mutation | CCT,TCT | P965S | XP_016869360.1 |