ENST00000215882.10:c.566T>G
MANE Select
|
ENSP00000215882.5:p.Leu189Arg
|
|
ENST00000215882.9:c.566T>G
|
ENSP00000215882.5:p.Leu189Arg
|
|
ENST00000451283.5:c.257T>G
|
ENSP00000401480.1:p.Leu86Arg
|
|
ENST00000461267.1:n.712T>G
|
|
|
ENST00000470922.5:n.708T>G
|
|
|
NM_001256534.1:c.587T>G
|
NP_001243463.1:p.Leu196Arg
|
|
NM_001287387.1:c.257T>G
|
NP_001274316.1:p.Leu86Arg
|
|
NM_005984.4:c.566T>G
|
NP_005975.1:p.Leu189Arg
|
|
NR_046298.2:n.617T>G
|
|
|
NM_005984.5:c.566T>G
MANE Select
|
NP_005975.1:p.Leu189Arg
|
|
NM_001256534.2:c.587T>G
|
NP_001243463.1:p.Leu196Arg
|
|
NM_001287387.2:c.257T>G
|
NP_001274316.1:p.Leu86Arg
|
|
NR_046298.3:n.490T>G
|
|
|