ENST00000328300.11:c.5048G=
MANE Select
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ENSP00000331902.7:p.Arg1683=
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ENST00000361603.7:c.5030G=
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ENSP00000354505.2:p.Arg1677=
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ENST00000510690.2:n.1542G=
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ENST00000644079.1:n.2736G=
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ENST00000328300.10:c.5048G=
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ENSP00000331902.6:p.Arg1683=
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ENST00000361603.6:c.5030G=
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ENSP00000354505.2:p.Arg1677=
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ENST00000504541.1:c.273G=
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ENSP00000424845.1:n.273G=
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ENST00000515658.1:c.378G=
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NM_000495.4:c.5030G=
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NP_000486.1:p.Arg1677=
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NM_033380.2:c.5048G=
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NP_203699.1:p.Arg1683=
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XM_005262070.2:c.5039G=
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XP_005262127.1:p.Arg1680=
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XM_006724616.2:c.5048G=
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XP_006724679.1:p.Arg1683=
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XM_011530849.1:c.4724G=
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XP_011529151.1:p.Arg1575=
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XM_011530851.1:c.2621G=
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XP_011529153.1:p.Arg874=
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XM_011530849.2:c.5063G=
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XP_011529151.2:p.Arg1688=
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XM_017029259.2:c.5054G=
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XP_016884748.1:p.Arg1685=
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XM_017029260.1:c.5045G=
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XP_016884749.1:p.Arg1682=
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XM_017029263.2:c.3383G=
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XP_016884752.1:p.Arg1128=
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NM_000495.5:c.5030G=
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NP_000486.1:p.Arg1677=
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NM_033380.3:c.5048G=
MANE Select
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NP_203699.1:p.Arg1683=
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