Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001007469.1 | 228 | Silent Mutation | TCC,TCT | S38S | NP_001007470.1 |
NM_014266.3 | 228 | Silent Mutation | TCC,TCT | S38S | NP_055081.1 |
XM_017026193.1 | 228 | Missense Mutation | CCT,CTT | P79L | XP_016881682.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001173514.1 | 228 | Intron | NP_001166985.1 | ||
NM_001173515.1 | 228 | Intron | NP_001166986.1 | ||
NM_003332.3 | 228 | Intron | NP_003323.1 | ||
NM_198125.2 | 228 | Intron | NP_937758.1 |