ENST00000328300.11:c.4806T>C
MANE Select
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ENSP00000331902.7:p.Gly1602=
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ENST00000361603.7:c.4788T>C
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ENSP00000354505.2:p.Gly1596=
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ENST00000510690.2:n.1300T>C
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ENST00000644079.1:n.1292T>C
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ENST00000328300.10:c.4806T>C
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ENSP00000331902.6:p.Gly1602=
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ENST00000361603.6:c.4788T>C
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ENSP00000354505.2:p.Gly1596=
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ENST00000504541.1:c.204T>C
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ENSP00000424845.1:p.Gly68=
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ENST00000515658.1:c.325-1391T>C
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NM_000495.4:c.4788T>C
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NP_000486.1:p.Gly1596=
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NM_033380.2:c.4806T>C
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NP_203699.1:p.Gly1602=
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XM_005262070.2:c.4797T>C
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XP_005262127.1:p.Gly1599=
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XM_006724616.2:c.4806T>C
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XP_006724679.1:p.Gly1602=
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XM_011530849.1:c.4482T>C
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XP_011529151.1:p.Gly1494=
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XM_011530851.1:c.2379T>C
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XP_011529153.1:p.Gly793=
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XM_011530849.2:c.4821T>C
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XP_011529151.2:p.Gly1607=
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XM_017029259.2:c.4812T>C
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XP_016884748.1:p.Gly1604=
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XM_017029260.1:c.4803T>C
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XP_016884749.1:p.Gly1601=
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XM_017029263.2:c.3141T>C
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XP_016884752.1:p.Gly1047=
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NM_000495.5:c.4788T>C
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NP_000486.1:p.Gly1596=
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NM_033380.3:c.4806T>C
MANE Select
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NP_203699.1:p.Gly1602=
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