ENST00000309755.9:c.920G>C
MANE Select
|
ENSP00000312397.4:p.Gly307Ala
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ENST00000309755.8:c.920G>C
|
ENSP00000312397.4:p.Gly307Ala
|
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ENST00000502381.1:n.507G>C
|
|
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ENST00000504208.5:c.*335-11524G>C
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ENSP00000423585.1:n.*335-11524G>C
|
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ENST00000505853.1:c.800G>C
|
ENSP00000426173.1:p.Gly267Ala
|
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ENST00000506491.5:c.674G>C
|
ENSP00000424828.1:p.Gly225Ala
|
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ENST00000506873.5:n.545G>C
|
|
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ENST00000508657.5:c.824G>C
|
ENSP00000422099.1:p.Gly275Ala
|
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NM_001257194.1:c.824G>C
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NP_001244123.1:p.Gly275Ala
|
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NM_001257195.1:c.674G>C
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NP_001244124.1:p.Gly225Ala
|
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NM_017415.2:c.920G>C
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NP_059111.2:p.Gly307Ala
|
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NM_017415.3:c.920G>C
MANE Select
|
NP_059111.2:p.Gly307Ala
|
|
NM_001257195.2:c.674G>C
|
NP_001244124.1:p.Gly225Ala
|
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