ENST00000268125.10:c.589G>T
MANE Select
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ENSP00000268125.5:p.Gly197Cys
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ENST00000268125.9:c.589G>T
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ENSP00000268125.5:p.Gly197Cys
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ENST00000563254.1:c.6G>T
|
|
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ENST00000567787.1:c.*167G>T
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ENSP00000457251.1:n.*167G>T
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NM_000326.4:c.589G>T
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NP_000317.1:p.Gly197Cys
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XM_011521870.1:c.589G>T
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XP_011520172.1:p.Gly197Cys
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XM_011521871.1:c.514G>T
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XP_011520173.1:p.Gly172Cys
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XM_011521872.1:c.514G>T
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XP_011520174.1:p.Gly172Cys
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XM_011521870.2:c.589G>T
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XP_011520172.1:p.Gly197Cys
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XM_017022460.1:c.616G>T
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XP_016877949.1:p.Gly206Cys
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NM_000326.5:c.589G>T
MANE Select
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NP_000317.1:p.Gly197Cys
|
|