Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001289135.2 | 1915 | Missense Mutation | CGC,TGC | R2C | NP_001276064.1 |
NM_001289136.2 | 1915 | Missense Mutation | CGC,TGC | R2C | NP_001276065.1 |
NM_004787.3 | 1915 | Missense Mutation | CGC,TGC | R2C | NP_004778.1 |
XM_005248211.3 | 1915 | Missense Mutation | CGC,TGC | R2C | XP_005248268.1 |
XM_006713986.3 | 1915 | Missense Mutation | CGC,TGC | R2C | XP_006714049.1 |
XM_011513909.2 | 1915 | Intron | XP_011512211.1 | ||
XM_011513910.2 | 1915 | Intron | XP_011512212.2 | ||
XM_017008845.1 | 1915 | Intron | XP_016864334.1 |