Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001271667.1 | 1091 | Missense Mutation | ACC,AGC | T220S | NP_001258596.1 |
NM_001271668.1 | 1091 | Missense Mutation | ACC,AGC | T284S | NP_001258597.1 |
NM_001271669.1 | 1091 | Missense Mutation | ACC,AGC | T266S | NP_001258598.1 |
NM_032122.4 | 1091 | Missense Mutation | ACC,AGC | T301S | NP_115498.2 |
NM_183040.2 | 1091 | Intron | NP_898861.1 | ||
XM_005249447.4 | 1091 | Missense Mutation | ACC,AGC | T288S | XP_005249504.1 |
XM_011514936.2 | 1091 | Missense Mutation | ACC,AGC | T271S | XP_011513238.1 |
XM_011514937.2 | 1091 | Missense Mutation | ACC,AGC | T145S | XP_011513239.1 |
XM_017011348.1 | 1091 | Missense Mutation | ACC,AGC | T151S | XP_016866837.1 |
XM_017011349.1 | 1091 | Missense Mutation | ACC,AGC | T150S | XP_016866838.1 |