ENST00000215882.10:c.585G=
MANE Select
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ENSP00000215882.5:p.Gln195=
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|
ENST00000215882.9:c.585G=
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ENSP00000215882.5:p.Gln195=
|
|
ENST00000451283.5:c.276G=
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ENSP00000401480.1:p.Gln92=
|
|
ENST00000461267.1:n.731G=
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|
|
ENST00000470922.5:n.727G=
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|
|
NM_001256534.1:c.606G=
|
NP_001243463.1:p.Gln202=
|
|
NM_001287387.1:c.276G=
|
NP_001274316.1:p.Gln92=
|
|
NM_005984.4:c.585G=
|
NP_005975.1:p.Gln195=
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NR_046298.2:n.636G=
|
|
|
NM_005984.5:c.585G=
MANE Select
|
NP_005975.1:p.Gln195=
|
|
NM_001256534.2:c.606G=
|
NP_001243463.1:p.Gln202=
|
|
NM_001287387.2:c.276G=
|
NP_001274316.1:p.Gln92=
|
|
NR_046298.3:n.509G=
|
|
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