ENST00000644269.2:c.1444T>G
MANE Select
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ENSP00000494017.1:p.Trp482Gly
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ENST00000644846.1:c.155T>G
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ENST00000265715.7:c.1444T>G
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ENSP00000265715.3:p.Trp482Gly
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ENST00000460748.1:n.547T>G
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ENST00000477350.5:n.291T>G
|
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ENST00000480841.5:n.293T>G
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ENST00000497446.5:n.459T>G
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NM_000441.1:c.1444T>G
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NP_000432.1:p.Trp482Gly
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XM_005250425.1:c.1444T>G
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XP_005250482.1:p.Trp482Gly
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XM_005250425.2:c.1444T>G
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XP_005250482.1:p.Trp482Gly
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XM_017012318.1:c.1366T>G
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XP_016867807.1:p.Trp456Gly
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NM_000441.2:c.1444T>G
MANE Select
|
NP_000432.1:p.Trp482Gly
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