ENST00000215882.10:c.527-41C>G
MANE Select
|
ENSP00000215882.5:n.527-41C>G
|
|
ENST00000215882.9:c.527-41C>G
|
ENSP00000215882.5:n.527-41C>G
|
|
ENST00000451283.5:c.218-41C>G
|
ENSP00000401480.1:n.218-41C>G
|
|
ENST00000461267.1:n.673-41C>G
|
|
|
ENST00000470922.5:n.669-41C>G
|
|
|
NM_001256534.1:c.548-41C>G
|
NP_001243463.1:n.548-41C>G
|
|
NM_001287387.1:c.218-41C>G
|
NP_001274316.1:n.218-41C>G
|
|
NM_005984.4:c.527-41C>G
|
NP_005975.1:n.527-41C>G
|
|
NR_046298.2:n.578-41C>G
|
|
|
NM_005984.5:c.527-41C>G
MANE Select
|
NP_005975.1:n.527-41C>G
|
|
NM_001256534.2:c.548-41C>G
|
NP_001243463.1:n.548-41C>G
|
|
NM_001287387.2:c.218-41C>G
|
NP_001274316.1:n.218-41C>G
|
|
NR_046298.3:n.451-41C>G
|
|
|