ENST00000433363.7:c.911A>T
MANE Select
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ENSP00000406220.2:p.Glu304Val
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ENST00000293800.10:c.860A>T
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ENSP00000293800.6:p.Glu287Val
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ENST00000381074.8:c.782A>T
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ENSP00000370464.4:p.Glu261Val
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ENST00000433363.6:c.911A>T
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ENSP00000406220.2:p.Glu304Val
|
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ENST00000572094.1:c.*661A>T
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ENSP00000461495.1:n.*661A>T
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ENST00000572727.1:n.20A>T
|
|
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ENST00000573648.5:c.911A>T
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ENSP00000459372.1:p.Glu304Val
|
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ENST00000574824.5:n.2044A>T
|
|
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NM_001143838.2:c.911A>T
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NP_001137310.1:p.Glu304Val
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NM_001284509.1:c.860A>T
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NP_001271438.1:p.Glu287Val
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NM_001284510.1:c.782A>T
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NP_001271439.1:p.Glu261Val
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NM_177550.4:c.911A>T , LRG_1020t1:c.911A>T
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NP_808218.1:p.Glu304Val
|
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XM_006721504.2:c.800A>T
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XP_006721567.1:p.Glu267Val
|
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XM_011523795.1:c.911A>T
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XP_011522097.1:p.Glu304Val
|
|
XM_011523795.3:c.911A>T
|
XP_011522097.1:p.Glu304Val
|
|
NM_001143838.3:c.911A>T
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NP_001137310.1:p.Glu304Val
|
|
NM_001284509.2:c.860A>T
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NP_001271438.1:p.Glu287Val
|
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NM_001284510.2:c.782A>T
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NP_001271439.1:p.Glu261Val
|
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NM_177550.5:c.911A>T
MANE Select
|
NP_808218.1:p.Glu304Val
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