ENST00000263967.4:c.3138A>C
MANE Select
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ENSP00000263967.3:p.Ala1046=
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ENST00000462255.2:n.2161A>C
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ENST00000643187.1:c.*218A>C
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ENSP00000493507.1:n.*218A>C
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ENST00000674534.1:n.4046A>C
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ENST00000674622.1:c.1559A>C
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ENSP00000502417.1:n.1559A>C
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ENST00000675467.1:n.5945A>C
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ENST00000675786.1:c.*1705A>C
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ENSP00000502323.1:n.*1705A>C
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ENST00000675796.1:n.3033A>C
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ENST00000263967.3:c.3138A>C
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ENSP00000263967.3:p.Ala1046=
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NM_006218.2:c.3138A>C , LRG_310t1:c.3138A>C
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NP_006209.2:p.Ala1046=
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XM_006713658.2:c.3138A>C
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XP_006713721.1:p.Ala1046=
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XM_011512894.1:c.3138A>C
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XP_011511196.1:p.Ala1046=
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NM_006218.3:c.3138A>C
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NP_006209.2:p.Ala1046=
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XM_006713658.4:c.3138A>C
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XP_006713721.1:p.Ala1046=
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XM_011512894.2:c.3138A>C
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XP_011511196.1:p.Ala1046=
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NM_006218.4:c.3138A>C
MANE Select
|
NP_006209.2:p.Ala1046=
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