ENST00000296585.10:c.829G>A
MANE Select
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ENSP00000296585.5:p.Val277Ile
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|
ENST00000296585.9:c.829G>A
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ENSP00000296585.5:p.Val277Ile
|
|
ENST00000503810.6:c.*173G>A
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ENSP00000426489.1:n.*173G>A
|
|
ENST00000509814.5:c.829G>A
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ENSP00000424397.1:p.Val277Ile
|
|
ENST00000509960.5:c.829G>A
|
ENSP00000424642.1:p.Val277Ile
|
|
ENST00000510722.1:c.829G>A
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ENSP00000422145.1:p.Val277Ile
|
|
ENST00000513685.5:c.*543G>A
|
ENSP00000422095.1:n.*543G>A
|
|
NM_002203.3:c.829G>A
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NP_002194.2:p.Val277Ile
|
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NR_073103.1:n.972G>A
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|
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NR_073104.1:n.972G>A
|
|
|
NR_073105.1:n.972G>A
|
|
|
NR_073106.1:n.972G>A
|
|
|
NR_073107.1:n.851G>A
|
|
|
NM_002203.4:c.829G>A
MANE Select
|
NP_002194.2:p.Val277Ile
|
|
NR_073103.2:n.946G>A
|
|
|
NR_073104.2:n.946G>A
|
|
|
NR_073105.2:n.946G>A
|
|
|
NR_073106.2:n.946G>A
|
|
|
NR_073107.2:n.825G>A
|
|
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