Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001164840.2 | 121 | Intron | NP_001158312.1 | ||
NM_001164841.2 | 121 | Intron | NP_001158313.1 | ||
NM_001318782.1 | 121 | Intron | NP_001305711.1 | ||
NM_001318783.1 | 121 | Intron | NP_001305712.1 | ||
NM_020408.5 | 121 | Intron | NP_065141.3 | ||
XM_017011083.1 | 121 | Intron | XP_016866572.1 | ||
XM_017011084.1 | 121 | Intron | XP_016866573.1 |
Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001145115.2 | 121 | Missense Mutation | CGC,GGC | R41G | NP_001138587.1 |