Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001136.4 | 1050 | Missense Mutation | TCT,TGT | S301C | NP_001127.1 |
NM_001206929.1 | 1050 | Missense Mutation | TCT,TGT | S317C | NP_001193858.1 |
NM_001206932.1 | 1050 | Missense Mutation | TCT,TGT | S287C | NP_001193861.1 |
NM_001206934.1 | 1050 | Missense Mutation | TCT,TGT | S317C | NP_001193863.1 |
NM_001206936.1 | 1050 | Missense Mutation | CTG,GTG | L284V | NP_001193865.1 |
NM_001206940.1 | 1050 | Missense Mutation | TCT,TGT | S301C | NP_001193869.1 |
NM_001206954.1 | 1050 | Intron | NP_001193883.1 | ||
NM_001206966.1 | 1050 | Missense Mutation | TCT,TGT | S301C | NP_001193895.1 |
NM_172197.2 | 1050 | Intron | NP_751947.1 | ||
XM_017010328.1 | 1050 | Intron | XP_016865817.1 |