ENST00000342741.6:c.1627C=
MANE Select
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ENSP00000339933.4:p.Arg543=
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ENST00000342741.4:c.1627C=
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ENSP00000339933.4:p.Arg543=
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ENST00000392414.7:c.1534C=
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ENSP00000376214.3:p.Arg512=
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NM_000298.5:c.1627C=
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NP_000289.1:p.Arg543=
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NM_181871.3:c.1534C=
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NP_870986.1:p.Arg512=
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XM_005245266.3:c.1786C=
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XP_005245323.1:p.Arg596=
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XM_006711386.2:c.1435C=
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XP_006711449.1:p.Arg479=
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XM_011509640.1:c.1435C=
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XP_011507942.1:p.Arg479=
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NM_000298.6:c.1627C=
MANE Select
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NP_000289.1:p.Arg543=
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XM_006711386.4:c.1435C=
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XP_006711449.1:p.Arg479=
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XM_011509640.3:c.1435C=
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XP_011507942.1:p.Arg479=
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NM_181871.4:c.1534C=
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NP_870986.1:p.Arg512=
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