Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_199287.2 | 201 | Missense Mutation | CGC,CTC | R44L | NP_954981.1 |
XM_011524738.2 | 201 | Intron | XP_011523040.1 | ||
XM_017024573.1 | 201 | Missense Mutation | CGC,CTC | R60L | XP_016880062.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001039842.2 | 201 | Intron | NP_001034931.1 | ||
NM_001304994.1 | 201 | Intron | NP_001291923.1 | ||
NM_001304995.1 | 201 | Intron | NP_001291924.1 | ||
NM_001304999.1 | 201 | Intron | NP_001291928.1 |