ENST00000295897.9:c.1133A>C
MANE Select
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ENSP00000295897.4:p.Glu378Ala
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ENST00000295897.8:c.1133A>C
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ENSP00000295897.4:p.Glu378Ala
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ENST00000401494.7:c.788A>C
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ENSP00000384695.3:p.Glu263Ala
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ENST00000415165.6:c.557A>C
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ENSP00000401820.2:p.Glu186Ala
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ENST00000476441.6:c.*412A>C
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ENSP00000423727.1:n.*412A>C
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ENST00000484992.1:n.453A>C
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ENST00000503124.5:c.683A>C
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ENSP00000421027.1:p.Glu228Ala
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ENST00000504043.1:n.136A>C
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ENST00000505649.5:n.819A>C
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ENST00000509063.5:c.1133A>C
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ENSP00000422784.1:p.Glu378Ala
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ENST00000511370.1:c.666A>C
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ENST00000621085.4:c.494A>C
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ENSP00000483421.1:p.Glu165Ala
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ENST00000621628.4:c.494A>C
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ENSP00000480485.1:p.Glu165Ala
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NM_000477.5:c.1133A>C
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NP_000468.1:p.Glu378Ala
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NM_000477.6:c.1133A>C
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NP_000468.1:p.Glu378Ala
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NM_000477.7:c.1133A>C
MANE Select
|
NP_000468.1:p.Glu378Ala
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