ENST00000328300.11:c.4536T>C
MANE Select
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ENSP00000331902.7:p.Ala1512=
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ENST00000361603.7:c.4518T>C
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ENSP00000354505.2:p.Ala1506=
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ENST00000510690.2:n.1030T>C
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ENST00000328300.10:c.4536T>C
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ENSP00000331902.6:p.Ala1512=
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ENST00000361603.6:c.4518T>C
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ENSP00000354505.2:p.Ala1506=
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ENST00000515658.1:c.325-3542T>C
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NM_000495.4:c.4518T>C
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NP_000486.1:p.Ala1506=
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NM_033380.2:c.4536T>C
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NP_203699.1:p.Ala1512=
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XM_005262070.2:c.4527T>C
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XP_005262127.1:p.Ala1509=
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XM_006724616.2:c.4536T>C
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XP_006724679.1:p.Ala1512=
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XM_011530849.1:c.4212T>C
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XP_011529151.1:p.Ala1404=
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XM_011530851.1:c.2109T>C
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XP_011529153.1:p.Ala703=
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XM_011530849.2:c.4551T>C
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XP_011529151.2:p.Ala1517=
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XM_017029259.2:c.4542T>C
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XP_016884748.1:p.Ala1514=
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XM_017029260.1:c.4533T>C
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XP_016884749.1:p.Ala1511=
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XM_017029263.2:c.2871T>C
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XP_016884752.1:p.Ala957=
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NM_000495.5:c.4518T>C
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NP_000486.1:p.Ala1506=
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NM_033380.3:c.4536T>C
MANE Select
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NP_203699.1:p.Ala1512=
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