ENST00000426263.10:c.445C>G
MANE Select
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ENSP00000416293.2:p.Pro149Ala
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ENST00000674765.1:c.445C>G
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ENSP00000501811.1:p.Pro149Ala
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ENST00000675112.1:n.468C>G
|
|
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ENST00000676254.1:n.894C>G
|
|
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ENST00000426263.7:c.445C>G
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ENSP00000416293.2:p.Pro149Ala
|
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ENST00000439722.2:c.324C>G
|
ENSP00000395521.2:n.324C>G
|
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ENST00000475162.3:c.344C>G
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|
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ENST00000625233.2:n.653C>G
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|
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ENST00000630287.2:c.445C>G
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ENSP00000486694.1:p.Pro149Ala
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NM_006516.2:c.445C>G
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NP_006507.2:p.Pro149Ala
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NM_006516.3:c.445C>G
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NP_006507.2:p.Pro149Ala
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NM_006516.4:c.445C>G
MANE Select
|
NP_006507.2:p.Pro149Ala
|
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