ENST00000302068.9:c.1161A>G
MANE Select
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ENSP00000306099.4:p.Ala387=
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ENST00000302068.8:c.1161A>G
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ENSP00000306099.4:p.Ala387=
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ENST00000502545.5:n.939+409A>G
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ENST00000509493.1:c.504A>G
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ENSP00000426757.1:p.Ala168=
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NM_001184741.1:c.984A>G
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NP_001171670.1:p.Ala328=
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NM_005141.4:c.1161A>G , LRG_558t1:c.1161A>G
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NP_005132.2:p.Ala387=
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NM_001382759.1:c.1029A>G
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NP_001369688.1:p.Ala343=
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NM_001382760.1:c.1161A>G
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NP_001369689.1:p.Ala387=
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NM_001382761.1:c.1161A>G
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NP_001369690.1:p.Ala387=
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NM_001382762.1:c.861A>G
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NP_001369691.1:p.Ala287=
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NM_001382763.1:c.1152A>G
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NP_001369692.1:p.Ala384=
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NM_001382764.1:c.1081-57A>G
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NP_001369693.1:n.1081-57A>G
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NM_001382765.1:c.1161A>G
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NP_001369694.1:p.Ala387=
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NM_005141.5:c.1161A>G
MANE Select
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NP_005132.2:p.Ala387=
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