ENST00000328300.11:c.4837G>T
MANE Select
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ENSP00000331902.7:p.Ala1613Ser
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ENST00000361603.7:c.4819G>T
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ENSP00000354505.2:p.Ala1607Ser
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ENST00000510690.2:n.1331G>T
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ENST00000644079.1:n.1668G>T
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ENST00000328300.10:c.4837G>T
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ENSP00000331902.6:p.Ala1613Ser
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ENST00000361603.6:c.4819G>T
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ENSP00000354505.2:p.Ala1607Ser
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ENST00000504541.1:c.219+361G>T
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ENSP00000424845.1:n.219+361G>T
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ENST00000515658.1:c.325-1015G>T
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NM_000495.4:c.4819G>T
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NP_000486.1:p.Ala1607Ser
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NM_033380.2:c.4837G>T
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NP_203699.1:p.Ala1613Ser
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XM_005262070.2:c.4828G>T
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XP_005262127.1:p.Ala1610Ser
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XM_006724616.2:c.4837G>T
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XP_006724679.1:p.Ala1613Ser
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XM_011530849.1:c.4513G>T
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XP_011529151.1:p.Ala1505Ser
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XM_011530851.1:c.2410G>T
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XP_011529153.1:p.Ala804Ser
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XM_011530849.2:c.4852G>T
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XP_011529151.2:p.Ala1618Ser
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XM_017029259.2:c.4843G>T
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XP_016884748.1:p.Ala1615Ser
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XM_017029260.1:c.4834G>T
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XP_016884749.1:p.Ala1612Ser
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XM_017029263.2:c.3172G>T
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XP_016884752.1:p.Ala1058Ser
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NM_000495.5:c.4819G>T
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NP_000486.1:p.Ala1607Ser
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NM_033380.3:c.4837G>T
MANE Select
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NP_203699.1:p.Ala1613Ser
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