ENST00000367435.5:c.1025G>C
MANE Select
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ENSP00000356405.4:p.Arg342Thr
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|
ENST00000635846.1:c.782G>C
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ENSP00000490035.1:p.Arg261Thr
|
|
ENST00000643006.1:c.1093G>C
|
ENSP00000496633.1:p.Asp365His
|
|
ENST00000648071.1:c.*1001G>C
|
ENSP00000497513.1:n.*1001G>C
|
|
ENST00000649613.1:n.275G>C
|
|
|
ENST00000649895.1:n.1243G>C
|
|
|
ENST00000650197.1:c.1025G>C
|
ENSP00000496929.1:p.Arg342Thr
|
|
ENST00000367435.3:c.1025G>C
|
ENSP00000356405.3:p.Arg342Thr
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|
NM_024529.4:c.1025G>C , LRG_507t1:c.1025G>C
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NP_078805.3:p.Arg342Thr
|
|
NM_024529.5:c.1025G>C
MANE Select
|
NP_078805.3:p.Arg342Thr
|
|