ENST00000706645.1:n.1493G>C
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ENST00000281243.10:c.446G>C
MANE Select
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ENSP00000281243.5:p.Gly149Ala
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ENST00000281243.9:c.446G>C
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ENSP00000281243.5:p.Gly149Ala
|
|
ENST00000428702.6:c.353G>C
|
ENSP00000390944.2:p.Gly118Ala
|
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ENST00000501943.6:n.183G>C
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ENST00000505710.1:c.364-1586G>C
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ENST00000507439.5:c.437-1586G>C
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ENSP00000423227.1:n.437-1586G>C
|
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ENST00000508623.5:c.437-5095G>C
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ENSP00000426377.1:n.437-5095G>C
|
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ENST00000511609.1:n.178G>C
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ENST00000513615.5:c.437-1586G>C
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ENSP00000422759.1:n.437-1586G>C
|
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ENST00000514300.1:c.*368-1586G>C
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ENSP00000426039.1:n.*368-1586G>C
|
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NM_000320.2:c.446G>C
|
NP_000311.2:p.Gly149Ala
|
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NM_001306140.1:c.353G>C
|
NP_001293069.1:p.Gly118Ala
|
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XR_241677.1:n.600-1586G>C
|
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NR_156494.1:n.617-1586G>C
|
|
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NM_000320.3:c.446G>C
MANE Select
|
NP_000311.2:p.Gly149Ala
|
|
NM_001306140.2:c.353G>C
|
NP_001293069.1:p.Gly118Ala
|
|
NR_156494.2:n.473-1586G>C
|
|
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