ENST00000328300.11:c.4925G>T
MANE Select
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ENSP00000331902.7:p.Gly1642Val
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ENST00000361603.7:c.4907G>T
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ENSP00000354505.2:p.Gly1636Val
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ENST00000510690.2:n.1419G>T
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ENST00000644079.1:n.1756G>T
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ENST00000328300.10:c.4925G>T
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ENSP00000331902.6:p.Gly1642Val
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ENST00000361603.6:c.4907G>T
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ENSP00000354505.2:p.Gly1636Val
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ENST00000504541.1:c.219+449G>T
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ENSP00000424845.1:n.219+449G>T
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ENST00000515658.1:c.325-927G>T
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NM_000495.4:c.4907G>T
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NP_000486.1:p.Gly1636Val
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NM_033380.2:c.4925G>T
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NP_203699.1:p.Gly1642Val
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XM_005262070.2:c.4916G>T
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XP_005262127.1:p.Gly1639Val
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XM_006724616.2:c.4925G>T
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XP_006724679.1:p.Gly1642Val
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XM_011530849.1:c.4601G>T
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XP_011529151.1:p.Gly1534Val
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XM_011530851.1:c.2498G>T
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XP_011529153.1:p.Gly833Val
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XM_011530849.2:c.4940G>T
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XP_011529151.2:p.Gly1647Val
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XM_017029259.2:c.4931G>T
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XP_016884748.1:p.Gly1644Val
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XM_017029260.1:c.4922G>T
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XP_016884749.1:p.Gly1641Val
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XM_017029263.2:c.3260G>T
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XP_016884752.1:p.Gly1087Val
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NM_000495.5:c.4907G>T
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NP_000486.1:p.Gly1636Val
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NM_033380.3:c.4925G>T
MANE Select
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NP_203699.1:p.Gly1642Val
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