ENST00000400521.7:c.257G>A
MANE Select
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ENSP00000383365.1:p.Cys86Tyr
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ENST00000334363.14:c.257G>A
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ENSP00000334451.9:p.Cys86Tyr
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ENST00000400518.5:c.167G>A
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ENSP00000383362.1:p.Cys56Tyr
|
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ENST00000400519.6:c.254G>A
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ENSP00000383363.1:p.Cys85Tyr
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ENST00000400521.6:c.257G>A
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ENSP00000383365.1:p.Cys86Tyr
|
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ENST00000400525.6:c.188G>A
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ENSP00000383369.3:p.Cys63Tyr
|
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ENST00000474308.5:c.200G>A
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ENSP00000485665.1:p.Cys67Tyr
|
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ENST00000491939.6:c.161G>A
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ENSP00000485543.1:p.Cys54Tyr
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ENST00000496729.2:n.262G>A
|
|
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ENST00000542719.6:c.-32G>A
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ENSP00000485128.2:n.-32G>A
|
|
NM_001282512.1:c.257G>A
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NP_001269441.1:p.Cys86Tyr
|
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NM_006440.4:c.257G>A
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NP_006431.2:p.Cys86Tyr
|
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NM_001282512.2:c.257G>A
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NP_001269441.1:p.Cys86Tyr
|
|
NM_001352300.1:c.254G>A
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NP_001339229.1:p.Cys85Tyr
|
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NM_001352301.1:c.167G>A
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NP_001339230.1:p.Cys56Tyr
|
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NM_001352302.1:c.-32G>A
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NP_001339231.1:n.-32G>A
|
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NM_001352303.1:c.161G>A
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NP_001339232.1:p.Cys54Tyr
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NR_147957.1:n.389G>A
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|
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NM_006440.5:c.257G>A
MANE Select
|
NP_006431.2:p.Cys86Tyr
|
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NM_001282512.3:c.257G>A
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NP_001269441.1:p.Cys86Tyr
|
|
NM_001352300.2:c.254G>A
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NP_001339229.1:p.Cys85Tyr
|
|
NR_147957.2:n.215G>A
|
|
|
NM_001352301.2:c.167G>A
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NP_001339230.1:p.Cys56Tyr
|
|
NM_001352302.2:c.-32G>A
|
NP_001339231.1:n.-32G>A
|
|
NM_001352303.2:c.161G>A
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NP_001339232.1:p.Cys54Tyr
|
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