ENST00000399503.4:c.2542C=
MANE Select
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ENSP00000382423.3:p.His848=
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ENST00000399503.3:c.2542C=
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ENSP00000382423.3:p.His848=
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NM_005921.1:c.2542C=
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NP_005912.1:p.His848=
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XM_005248519.3:c.2164C=
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XP_005248576.2:p.His722=
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XM_011543406.1:c.2287C=
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XP_011541708.1:p.His763=
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XM_011543407.1:c.2263C=
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XP_011541709.1:p.His755=
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XM_011543408.1:c.2542C=
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XP_011541710.1:p.His848=
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XM_017009484.1:c.2131C=
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XP_016864973.1:p.His711=
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XM_017009485.1:c.2053C=
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XP_016864974.1:p.His685=
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XR_001742068.2:n.2573C=
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|
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NM_005921.2:c.2542C=
MANE Select
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NP_005912.1:p.His848=
|
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