ENST00000217958.8:c.651T>G
MANE Select
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ENSP00000217958.3:p.Gly217=
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ENST00000217958.7:c.651T>G
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ENSP00000217958.3:p.Gly217=
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|
ENST00000340200.5:c.552T>G
|
ENSP00000345963.5:p.Gly184=
|
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ENST00000361815.9:c.*116T>G
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ENSP00000354906.5:n.*116T>G
|
|
ENST00000372295.5:c.528T>G
|
ENSP00000361369.1:p.Gly176=
|
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ENST00000372296.5:c.*116T>G
|
ENSP00000361370.1:n.*116T>G
|
|
NM_002814.3:c.651T>G
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NP_002805.1:p.Gly217=
|
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NM_170750.2:c.*116T>G
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NP_736606.1:n.*116T>G
|
|
NM_002814.4:c.651T>G
MANE Select
|
NP_002805.1:p.Gly217=
|
|
NM_170750.3:c.*116T>G
|
NP_736606.1:n.*116T>G
|
|