ENST00000426263.10:c.414C>G
MANE Select
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ENSP00000416293.2:p.Gly138=
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ENST00000674765.1:c.414C>G
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ENSP00000501811.1:p.Gly138=
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ENST00000675112.1:n.437C>G
|
|
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ENST00000676254.1:n.863C>G
|
|
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ENST00000372500.4:c.318C>G
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ENSP00000361578.4:p.Gly106=
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ENST00000426263.7:c.414C>G
|
ENSP00000416293.2:p.Gly138=
|
|
ENST00000439722.2:c.293C>G
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ENSP00000395521.2:n.293C>G
|
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ENST00000475162.3:c.313C>G
|
|
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ENST00000625233.2:n.622C>G
|
|
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ENST00000630287.2:c.414C>G
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ENSP00000486694.1:p.Gly138=
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NM_006516.2:c.414C>G
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NP_006507.2:p.Gly138=
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NM_006516.3:c.414C>G
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NP_006507.2:p.Gly138=
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|
NM_006516.4:c.414C>G
MANE Select
|
NP_006507.2:p.Gly138=
|
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