ENST00000215882.10:c.535G>A
MANE Select
|
ENSP00000215882.5:p.Gly179Arg
|
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ENST00000215882.9:c.535G>A
|
ENSP00000215882.5:p.Gly179Arg
|
|
ENST00000451283.5:c.226G>A
|
ENSP00000401480.1:p.Gly76Arg
|
|
ENST00000461267.1:n.681G>A
|
|
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ENST00000470922.5:n.677G>A
|
|
|
NM_001256534.1:c.556G>A
|
NP_001243463.1:p.Gly186Arg
|
|
NM_001287387.1:c.226G>A
|
NP_001274316.1:p.Gly76Arg
|
|
NM_005984.4:c.535G>A
|
NP_005975.1:p.Gly179Arg
|
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NR_046298.2:n.586G>A
|
|
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NM_005984.5:c.535G>A
MANE Select
|
NP_005975.1:p.Gly179Arg
|
|
NM_001256534.2:c.556G>A
|
NP_001243463.1:p.Gly186Arg
|
|
NM_001287387.2:c.226G>A
|
NP_001274316.1:p.Gly76Arg
|
|
NR_046298.3:n.459G>A
|
|
|