ENST00000261647.10:c.1129T>G
MANE Select
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ENSP00000261647.5:p.Ser377Ala
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ENST00000261647.9:c.1129T>G
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ENSP00000261647.5:p.Ser377Ala
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ENST00000465567.1:n.1523T>G
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|
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ENST00000470649.1:c.247+806T>G
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ENSP00000465627.1:n.247+806T>G
|
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ENST00000475723.5:c.1313T>G
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|
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ENST00000481107.1:n.1797T>G
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|
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ENST00000497842.6:n.1333T>G
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NM_001271420.1:c.808T>G
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NP_001258349.1:p.Ser270Ala
|
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NM_017775.3:c.1129T>G
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NP_060245.3:p.Ser377Ala
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XM_017024801.2:c.994+806T>G
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XP_016880290.2:n.994+806T>G
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XM_017024802.2:c.994+806T>G
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XP_016880291.2:n.994+806T>G
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NM_017775.4:c.1129T>G
MANE Select
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NP_060245.3:p.Ser377Ala
|
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NM_001271420.2:c.808T>G
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NP_001258349.1:p.Ser270Ala
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