ENST00000324856.13:c.5357A>T
MANE Select
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ENSP00000320485.7:p.Glu1786Val
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ENST00000374152.7:c.4208A>T
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ENSP00000363267.2:p.Glu1403Val
|
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ENST00000430799.7:c.4205A>T
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ENSP00000390317.3:p.Glu1402Val
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ENST00000466382.2:c.774A>T
|
|
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ENST00000636219.1:c.4211A>T
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ENSP00000489842.1:p.Glu1404Val
|
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ENST00000637788.1:n.1157A>T
|
|
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ENST00000324856.11:c.5357A>T
|
ENSP00000320485.7:p.Glu1786Val
|
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ENST00000374152.6:c.4208A>T
|
ENSP00000363267.2:p.Glu1403Val
|
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ENST00000430799.6:c.2046A>T
|
|
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ENST00000457599.6:c.4706A>T
|
ENSP00000387636.2:p.Glu1569Val
|
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ENST00000466382.1:c.774A>T
|
|
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ENST00000532781.1:c.855A>T
|
|
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NM_006015.4:c.5357A>T , LRG_875t1:c.5357A>T
|
NP_006006.3:p.Glu1786Val
|
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NM_139135.2:c.4706A>T
|
NP_624361.1:p.Glu1569Val
|
|
NM_006015.5:c.5357A>T
|
NP_006006.3:p.Glu1786Val
|
|
NM_139135.3:c.4706A>T
|
NP_624361.1:p.Glu1569Val
|
|
NM_006015.6:c.5357A>T
MANE Select
|
NP_006006.3:p.Glu1786Val
|
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NM_139135.4:c.4706A>T
|
NP_624361.1:p.Glu1569Val
|
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