ENST00000328300.11:c.4855G>T
MANE Select
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ENSP00000331902.7:p.Ala1619Ser
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ENST00000361603.7:c.4837G>T
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ENSP00000354505.2:p.Ala1613Ser
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ENST00000510690.2:n.1349G>T
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ENST00000644079.1:n.1686G>T
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ENST00000328300.10:c.4855G>T
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ENSP00000331902.6:p.Ala1619Ser
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ENST00000361603.6:c.4837G>T
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ENSP00000354505.2:p.Ala1613Ser
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ENST00000504541.1:c.219+379G>T
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ENSP00000424845.1:n.219+379G>T
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ENST00000515658.1:c.325-997G>T
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NM_000495.4:c.4837G>T
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NP_000486.1:p.Ala1613Ser
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NM_033380.2:c.4855G>T
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NP_203699.1:p.Ala1619Ser
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XM_005262070.2:c.4846G>T
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XP_005262127.1:p.Ala1616Ser
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XM_006724616.2:c.4855G>T
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XP_006724679.1:p.Ala1619Ser
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XM_011530849.1:c.4531G>T
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XP_011529151.1:p.Ala1511Ser
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XM_011530851.1:c.2428G>T
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XP_011529153.1:p.Ala810Ser
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XM_011530849.2:c.4870G>T
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XP_011529151.2:p.Ala1624Ser
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XM_017029259.2:c.4861G>T
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XP_016884748.1:p.Ala1621Ser
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XM_017029260.1:c.4852G>T
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XP_016884749.1:p.Ala1618Ser
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XM_017029263.2:c.3190G>T
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XP_016884752.1:p.Ala1064Ser
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NM_000495.5:c.4837G>T
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NP_000486.1:p.Ala1613Ser
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NM_033380.3:c.4855G>T
MANE Select
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NP_203699.1:p.Ala1619Ser
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