ENST00000373296.8:c.464T>G
MANE Select
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ENSP00000362393.3:p.Val155Gly
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ENST00000373294.8:c.464T>G
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ENSP00000362390.5:p.Val155Gly
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ENST00000373296.7:c.464T>G
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ENSP00000362393.3:p.Val155Gly
|
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ENST00000626498.2:c.*76T>G
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ENSP00000487527.1:n.*76T>G
|
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ENST00000626877.1:n.343T>G
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|
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NM_001109878.1:c.464T>G
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NP_001103348.1:p.Val155Gly
|
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NM_001109879.1:c.104T>G
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NP_001103349.1:p.Val35Gly
|
|
NM_001303475.1:c.104T>G
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NP_001290404.1:p.Val35Gly
|
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NM_016954.2:c.464T>G
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NP_058650.1:p.Val155Gly
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XM_005262136.2:c.467T>G
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XP_005262193.1:p.Val156Gly
|
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XM_006724657.2:c.467T>G
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XP_006724720.1:p.Val156Gly
|
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XM_011530972.1:c.104T>G
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XP_011529274.1:p.Val35Gly
|
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NM_001109878.2:c.464T>G
MANE Select
|
NP_001103348.1:p.Val155Gly
|
|
NM_001109879.2:c.104T>G
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NP_001103349.1:p.Val35Gly
|
|