NM_000732.6:c.411C>A
MANE Select
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NP_000723.1:p.Ala137=
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ENST00000300692.9:c.411C>A
MANE Select
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ENSP00000300692.4:p.Ala137=
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NM_000732.4:c.411C>A , LRG_37t1:c.411C>A
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NP_000723.1:p.Ala137=
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NM_001040651.1:c.279C>A
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NP_001035741.1:p.Ala93=
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NM_001040651.2:c.279C>A
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NP_001035741.1:p.Ala93=
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ENST00000300692.8:c.411C>A
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ENSP00000300692.4:p.Ala137=
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ENST00000392884.2:c.279C>A
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ENSP00000376622.2:p.Ala93=
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ENST00000526561.1:n.84C>A
|
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ENST00000529594.5:c.192C>A
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ENSP00000437335.1:p.Ala64=
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ENST00000534687.5:c.292C>A
|
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ENST00000695666.1:n.1178C>A
|
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ENST00000695667.1:n.696C>A
|
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