ENST00000367698.4:c.787C>G
MANE Select
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ENSP00000356671.3:p.Pro263Ala
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ENST00000367698.3:c.787C>G
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ENSP00000356671.3:p.Pro263Ala
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ENST00000487183.1:n.438C>G
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|
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ENST00000617423.4:c.559+1946C>G
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ENSP00000478688.1:n.559+1946C>G
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NM_000488.3:c.787C>G , LRG_577t1:c.787C>G
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NP_000479.1:p.Pro263Ala
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XM_005245198.2:c.643C>G
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XP_005245255.1:p.Pro215Ala
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NM_001365052.1:c.643C>G
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NP_001351981.1:p.Pro215Ala
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NM_000488.4:c.787C>G
MANE Select
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NP_000479.1:p.Pro263Ala
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NM_001365052.2:c.643C>G
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NP_001351981.1:p.Pro215Ala
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NM_001386302.1:c.910C>G
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NP_001373231.1:p.Pro304Ala
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NM_001386303.1:c.868C>G
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NP_001373232.1:p.Pro290Ala
|
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NM_001386304.1:c.766C>G
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NP_001373233.1:p.Pro256Ala
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NM_001386305.1:c.763-33C>G
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NP_001373234.1:n.763-33C>G
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NM_001386306.1:c.571C>G
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NP_001373235.1:p.Pro191Ala
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