Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
---|---|---|---|---|---|
NM_001199461.1 | 1135 | Intron | NP_001186390.1 | ||
NM_001199462.1 | 1135 | Missense Mutation | CAT,GAT | H309D | NP_001186391.1 |
NM_001199463.1 | 1135 | Intron | NP_001186392.1 | ||
NM_001199464.1 | 1135 | Intron | NP_001186393.1 | ||
NM_002598.3 | 1135 | Missense Mutation | CAT,GAT | H342D | NP_002589.2 |
NM_144781.2 | 1135 | Intron | NP_659005.1 | ||
XM_017010926.1 | 1135 | Intron | XP_016866415.1 |