ENST00000367435.5:c.679A>C
MANE Select
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ENSP00000356405.4:p.Arg227=
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ENST00000635846.1:c.679A>C
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ENSP00000490035.1:p.Arg227=
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ENST00000643006.1:c.679A>C
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ENSP00000496633.1:p.Arg227=
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ENST00000643784.1:c.*155A>C
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ENSP00000494944.1:n.*155A>C
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ENST00000647662.1:n.580A>C
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|
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ENST00000648071.1:c.*655A>C
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ENSP00000497513.1:n.*655A>C
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ENST00000649606.1:n.692A>C
|
|
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ENST00000649895.1:n.897A>C
|
|
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ENST00000650197.1:c.679A>C
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ENSP00000496929.1:p.Arg227=
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ENST00000367435.3:c.679A>C
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ENSP00000356405.3:p.Arg227=
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NM_024529.4:c.679A>C , LRG_507t1:c.679A>C
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NP_078805.3:p.Arg227=
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XM_006711537.2:c.679A>C
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XP_006711600.1:p.Arg227=
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XM_006711537.4:c.679A>C
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XP_006711600.1:p.Arg227=
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NM_024529.5:c.679A>C
MANE Select
|
NP_078805.3:p.Arg227=
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