ENST00000400521.7:c.798G>T
MANE Select
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ENSP00000383365.1:p.Glu266Asp
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ENST00000334363.14:c.798G>T
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ENSP00000334451.9:p.Glu266Asp
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ENST00000400518.5:c.708G>T
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ENSP00000383362.1:p.Glu236Asp
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ENST00000400519.6:c.795G>T
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ENSP00000383363.1:p.Glu265Asp
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ENST00000400521.6:c.798G>T
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ENSP00000383365.1:p.Glu266Asp
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ENST00000400525.6:c.729G>T
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ENSP00000383369.3:p.Glu243Asp
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ENST00000474308.5:c.741G>T
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ENSP00000485665.1:p.Glu247Asp
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ENST00000475995.3:c.295G>T
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|
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ENST00000491939.6:c.702G>T
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ENSP00000485543.1:p.Glu234Asp
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ENST00000494454.5:n.872G>T
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|
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ENST00000542719.6:c.510G>T
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ENSP00000485128.2:p.Glu170Asp
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ENST00000634537.1:c.27G>T
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ENSP00000489208.1:p.Glu9Asp
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ENST00000635155.1:n.384G>T
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|
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NM_001282512.1:c.798G>T
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NP_001269441.1:p.Glu266Asp
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NM_006440.4:c.798G>T
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NP_006431.2:p.Glu266Asp
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NM_001282512.2:c.798G>T
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NP_001269441.1:p.Glu266Asp
|
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NM_001352300.1:c.795G>T
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NP_001339229.1:p.Glu265Asp
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NM_001352301.1:c.708G>T
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NP_001339230.1:p.Glu236Asp
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NM_001352302.1:c.510G>T
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NP_001339231.1:p.Glu170Asp
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NM_001352303.1:c.702G>T
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NP_001339232.1:p.Glu234Asp
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NR_147957.1:n.930G>T
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|
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NM_006440.5:c.798G>T
MANE Select
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NP_006431.2:p.Glu266Asp
|
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NM_001282512.3:c.798G>T
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NP_001269441.1:p.Glu266Asp
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|
NM_001352300.2:c.795G>T
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NP_001339229.1:p.Glu265Asp
|
|
NR_147957.2:n.756G>T
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|
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NM_001352301.2:c.708G>T
|
NP_001339230.1:p.Glu236Asp
|
|
NM_001352302.2:c.510G>T
|
NP_001339231.1:p.Glu170Asp
|
|
NM_001352303.2:c.702G>T
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NP_001339232.1:p.Glu234Asp
|
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