Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001316973.1 | 732 | Missense Mutation | CAA,CCA | Q129P | NP_001303902.1 |
NM_001316974.1 | 732 | Missense Mutation | CAA,CCA | Q150P | NP_001303903.1 |
NM_001316975.1 | 732 | Missense Mutation | CAA,CCA | Q129P | NP_001303904.1 |
NM_001316976.1 | 732 | Intron | NP_001303905.1 | ||
NM_032368.4 | 732 | Missense Mutation | CAA,CCA | Q129P | NP_115744.2 |
XM_005263506.2 | 732 | Missense Mutation | CAA,CCA | Q129P | XP_005263563.1 |
XM_005263509.2 | 732 | Intron | XP_005263566.1 | ||
XM_017002546.1 | 732 | Missense Mutation | CAA,CCA | Q129P | XP_016858035.1 |
XM_017002547.1 | 732 | Missense Mutation | CAA,CCA | Q129P | XP_016858036.1 |