ENST00000296585.10:c.895T=
MANE Select
|
ENSP00000296585.5:p.Cys299=
|
|
ENST00000296585.9:c.895T=
|
ENSP00000296585.5:p.Cys299=
|
|
ENST00000503810.6:c.*239T=
|
ENSP00000426489.1:n.*239T=
|
|
ENST00000509814.5:c.895T=
|
ENSP00000424397.1:p.Cys299=
|
|
ENST00000509960.5:c.895T=
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ENSP00000424642.1:p.Cys299=
|
|
ENST00000510722.1:c.895T=
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ENSP00000422145.1:p.Cys299=
|
|
ENST00000513685.5:c.*609T=
|
ENSP00000422095.1:n.*609T=
|
|
NM_002203.3:c.895T=
|
NP_002194.2:p.Cys299=
|
|
NR_073103.1:n.1038T=
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|
|
NR_073104.1:n.1038T=
|
|
|
NR_073105.1:n.1038T=
|
|
|
NR_073106.1:n.1038T=
|
|
|
NR_073107.1:n.917T=
|
|
|
NM_002203.4:c.895T=
MANE Select
|
NP_002194.2:p.Cys299=
|
|
NR_073103.2:n.1012T=
|
|
|
NR_073104.2:n.1012T=
|
|
|
NR_073105.2:n.1012T=
|
|
|
NR_073106.2:n.1012T=
|
|
|
NR_073107.2:n.891T=
|
|
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