ENST00000367435.5:c.1026A>C
MANE Select
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ENSP00000356405.4:p.Arg342Ser
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ENST00000635846.1:c.783A>C
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ENSP00000490035.1:p.Arg261Ser
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ENST00000643006.1:c.1094A>C
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ENSP00000496633.1:p.Asp365Ala
|
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ENST00000648071.1:c.*1002A>C
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ENSP00000497513.1:n.*1002A>C
|
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ENST00000649613.1:n.276A>C
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|
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ENST00000649895.1:n.1244A>C
|
|
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ENST00000650197.1:c.1026A>C
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ENSP00000496929.1:p.Arg342Ser
|
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ENST00000367435.3:c.1026A>C
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ENSP00000356405.3:p.Arg342Ser
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NM_024529.4:c.1026A>C , LRG_507t1:c.1026A>C
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NP_078805.3:p.Arg342Ser
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NM_024529.5:c.1026A>C
MANE Select
|
NP_078805.3:p.Arg342Ser
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|