NM_002334.4:c.3830G=
MANE Select
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NP_002325.2:p.Arg1277=
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ENST00000378623.6:c.3830G=
MANE Select
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ENSP00000367888.1:p.Arg1277=
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NM_002334.3:c.3830G=
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NP_002325.2:p.Arg1277=
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ENST00000378623.5:c.3830G=
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ENSP00000367888.1:p.Arg1277=
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XM_011520102.1:c.4043G=
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XP_011518404.1:p.Arg1348=
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XM_011520103.1:c.3026G=
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XP_011518405.1:p.Arg1009=
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XM_011520103.2:c.3026G=
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XP_011518405.1:p.Arg1009=
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XM_011520104.1:c.1595G=
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XP_011518406.1:p.Arg532=
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XM_011520104.2:c.1595G=
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XP_011518406.1:p.Arg532=
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XM_017017734.1:c.3830G=
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XP_016873223.1:p.Arg1277=
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