ENST00000233190.11:c.1809T>G
MANE Select
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ENSP00000233190.5:p.Ala603=
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ENST00000233190.10:c.1809T>G
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ENSP00000233190.5:p.Ala603=
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ENST00000423725.5:c.1638T>G
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ENSP00000397760.1:p.Ala546=
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ENST00000432169.5:c.1476T>G
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ENSP00000409689.1:p.Ala492=
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ENST00000440274.5:c.1701T>G
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ENSP00000409766.1:p.Ala567=
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ENST00000449699.5:c.1809T>G
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ENSP00000399912.1:p.Ala603=
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ENST00000455934.6:c.1851T>G
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ENSP00000392709.2:p.Ala617=
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ENST00000457011.5:c.1461T>G
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ENSP00000400976.1:p.Ala487=
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ENST00000498520.1:n.281T>G
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NM_001199981.1:c.1701T>G
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NP_001186910.1:p.Ala567=
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NM_001199982.1:c.1476T>G
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NP_001186911.1:p.Ala492=
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NM_001199983.1:c.1638T>G
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NP_001186912.1:p.Ala546=
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NM_001199984.1:c.1851T>G
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NP_001186913.1:p.Ala617=
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NM_005006.6:c.1809T>G
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NP_004997.4:p.Ala603=
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XM_017004188.2:c.1050T>G
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XP_016859677.1:p.Ala350=
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NM_001199981.2:c.1701T>G
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NP_001186910.1:p.Ala567=
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NM_001199982.2:c.1476T>G
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NP_001186911.1:p.Ala492=
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NM_001199983.2:c.1638T>G
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NP_001186912.1:p.Ala546=
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NM_005006.7:c.1809T>G
MANE Select
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NP_004997.4:p.Ala603=
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NM_001199984.2:c.1851T>G
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NP_001186913.1:p.Ala617=
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