ENST00000328300.11:c.4919G>T
MANE Select
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ENSP00000331902.7:p.Gly1640Val
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ENST00000361603.7:c.4901G>T
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ENSP00000354505.2:p.Gly1634Val
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ENST00000510690.2:n.1413G>T
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ENST00000644079.1:n.1750G>T
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ENST00000328300.10:c.4919G>T
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ENSP00000331902.6:p.Gly1640Val
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ENST00000361603.6:c.4901G>T
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ENSP00000354505.2:p.Gly1634Val
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ENST00000504541.1:c.219+443G>T
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ENSP00000424845.1:n.219+443G>T
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ENST00000515658.1:c.325-933G>T
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NM_000495.4:c.4901G>T
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NP_000486.1:p.Gly1634Val
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NM_033380.2:c.4919G>T
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NP_203699.1:p.Gly1640Val
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XM_005262070.2:c.4910G>T
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XP_005262127.1:p.Gly1637Val
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XM_006724616.2:c.4919G>T
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XP_006724679.1:p.Gly1640Val
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XM_011530849.1:c.4595G>T
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XP_011529151.1:p.Gly1532Val
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XM_011530851.1:c.2492G>T
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XP_011529153.1:p.Gly831Val
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XM_011530849.2:c.4934G>T
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XP_011529151.2:p.Gly1645Val
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XM_017029259.2:c.4925G>T
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XP_016884748.1:p.Gly1642Val
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XM_017029260.1:c.4916G>T
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XP_016884749.1:p.Gly1639Val
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XM_017029263.2:c.3254G>T
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XP_016884752.1:p.Gly1085Val
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NM_000495.5:c.4901G>T
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NP_000486.1:p.Gly1634Val
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NM_033380.3:c.4919G>T
MANE Select
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NP_203699.1:p.Gly1640Val
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