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NM_001081.4:c.9229G>A
MANE Select
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NP_001072.2:p.Glu3077Lys
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|
ENST00000377833.10:c.9229G>A
MANE Select
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ENSP00000367064.4:p.Glu3077Lys
|
|
NM_001081.3:c.9229G>A , LRG_540t1:c.9229G>A
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NP_001072.2:p.Glu3077Lys
|
|
ENST00000377833.8:c.9229G>A
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ENSP00000367064.4:p.Glu3077Lys
|
|
XM_011519709.1:c.5215G>A
|
XP_011518011.1:p.Glu1739Lys
|
|
XM_011519709.2:c.5215G>A
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XP_011518011.1:p.Glu1739Lys
|
|
XM_011519710.1:c.5191G>A
|
XP_011518012.1:p.Glu1731Lys
|
|
XM_011519710.2:c.5191G>A
|
XP_011518012.1:p.Glu1731Lys
|
|
XM_011519711.1:c.5071G>A
|
XP_011518013.1:p.Glu1691Lys
|
|
XM_011519711.3:c.5071G>A
|
XP_011518013.1:p.Glu1691Lys
|