Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_181575.4 | 599 | Missense Mutation | TCC,TTC | S129F | NP_853553.1 |
XM_005264392.3 | 599 | Missense Mutation | TCC,TTC | S186F | XP_005264449.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001321727.1 | 599 | Intron | NP_001308656.1 | ||
NM_001321728.1 | 599 | Intron | NP_001308657.1 | ||
NM_013247.4 | 599 | Intron | NP_037379.1 | ||
NM_145074.2 | 599 | Intron | NP_659540.1 |