ENST00000328300.11:c.4943C>T
MANE Select
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ENSP00000331902.7:p.Ala1648Val
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ENST00000361603.7:c.4925C>T
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ENSP00000354505.2:p.Ala1642Val
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ENST00000510690.2:n.1437C>T
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ENST00000644079.1:n.1774C>T
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ENST00000328300.10:c.4943C>T
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ENSP00000331902.6:p.Ala1648Val
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ENST00000361603.6:c.4925C>T
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ENSP00000354505.2:p.Ala1642Val
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ENST00000504541.1:c.219+467C>T
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ENSP00000424845.1:n.219+467C>T
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ENST00000515658.1:c.325-909C>T
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NM_000495.4:c.4925C>T
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NP_000486.1:p.Ala1642Val
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NM_033380.2:c.4943C>T
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NP_203699.1:p.Ala1648Val
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XM_005262070.2:c.4934C>T
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XP_005262127.1:p.Ala1645Val
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XM_006724616.2:c.4943C>T
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XP_006724679.1:p.Ala1648Val
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XM_011530849.1:c.4619C>T
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XP_011529151.1:p.Ala1540Val
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XM_011530851.1:c.2516C>T
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XP_011529153.1:p.Ala839Val
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XM_011530849.2:c.4958C>T
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XP_011529151.2:p.Ala1653Val
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XM_017029259.2:c.4949C>T
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XP_016884748.1:p.Ala1650Val
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XM_017029260.1:c.4940C>T
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XP_016884749.1:p.Ala1647Val
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XM_017029263.2:c.3278C>T
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XP_016884752.1:p.Ala1093Val
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NM_000495.5:c.4925C>T
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NP_000486.1:p.Ala1642Val
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NM_033380.3:c.4943C>T
MANE Select
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NP_203699.1:p.Ala1648Val
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