Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_006493.2 | 599 | Missense Mutation | CGC,GGC | R191G | NP_006484.1 |
XM_011534917.2 | 599 | Missense Mutation | CGC,GGC | R191G | XP_011533219.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_012158.2 | 599 | Intron | NP_036290.1 | ||
XM_005266336.1 | 599 | Intron | XP_005266393.1 | ||
XM_005266337.2 | 599 | Intron | XP_005266394.1 | ||
XM_017020538.1 | 599 | Intron | XP_016876027.1 |