ENST00000316673.9:c.712G>C
MANE Select
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ENSP00000315180.4:p.Glu238Gln
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ENST00000316099.10:c.778G>C
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ENSP00000312987.3:p.Glu260Gln
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ENST00000619550.5:c.752G>C
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ENST00000683148.1:n.754G>C
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ENST00000683657.1:n.1902G>C
|
|
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ENST00000316099.9:c.778G>C
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ENSP00000312987.3:p.Glu260Gln
|
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ENST00000316099.8:c.778G>C
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ENSP00000312987.3:p.Glu260Gln
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ENST00000316673.8:c.712G>C
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ENSP00000315180.4:p.Glu238Gln
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ENST00000372920.1:c.*545G>C
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ENSP00000362011.1:n.*545G>C
|
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ENST00000415691.2:c.778G>C
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ENSP00000412111.1:p.Glu260Gln
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ENST00000443598.6:c.778G>C
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ENSP00000410911.2:p.Glu260Gln
|
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ENST00000457232.5:c.712G>C
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ENSP00000396216.1:p.Glu238Gln
|
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ENST00000609795.5:c.712G>C
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ENSP00000476609.1:p.Glu238Gln
|
|
ENST00000619550.4:c.703G>C
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ENSP00000481331.1:p.Glu235Gln
|
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NM_000457.4:c.778G>C , LRG_483t2:c.778G>C
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NP_000448.3:p.Glu260Gln
|
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NM_001030003.2:c.712G>C
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NP_001025174.1:p.Glu238Gln
|
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NM_001030004.2:c.712G>C
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NP_001025175.1:p.Glu238Gln
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NM_001258355.1:c.757G>C
|
NP_001245284.1:p.Glu253Gln
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NM_001287182.1:c.703G>C
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NP_001274111.1:p.Glu235Gln
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NM_001287183.1:c.703G>C , LRG_483t3:c.703G>C
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NP_001274112.1:p.Glu235Gln
|
|
NM_001287184.1:c.703G>C
|
NP_001274113.1:p.Glu235Gln
|
|
NM_175914.4:c.712G>C , LRG_483t1:c.712G>C
|
NP_787110.2:p.Glu238Gln
|
|
NM_178849.2:c.778G>C
|
NP_849180.1:p.Glu260Gln
|
|
NM_178850.2:c.778G>C
|
NP_849181.1:p.Glu260Gln
|
|
XM_005260407.2:c.895G>C
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XP_005260464.1:p.Glu299Gln
|
|
XM_011528797.1:c.826G>C
|
XP_011527099.1:p.Glu276Gln
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XM_011528798.1:c.826G>C
|
XP_011527100.1:p.Glu276Gln
|
|
XM_005260407.4:c.895G>C
|
XP_005260464.1:p.Glu299Gln
|
|
NM_001030003.3:c.712G>C
|
NP_001025174.1:p.Glu238Gln
|
|
NM_001030004.3:c.712G>C
|
NP_001025175.1:p.Glu238Gln
|
|
NM_001258355.2:c.757G>C
|
NP_001245284.1:p.Glu253Gln
|
|
NM_001287182.2:c.703G>C
|
NP_001274111.1:p.Glu235Gln
|
|
NM_001287184.2:c.703G>C
|
NP_001274113.1:p.Glu235Gln
|
|
NM_178849.3:c.778G>C
|
NP_849180.1:p.Glu260Gln
|
|
NM_178850.3:c.778G>C
|
NP_849181.1:p.Glu260Gln
|
|
NM_000457.5:c.778G>C
|
NP_000448.3:p.Glu260Gln
|
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NM_000457.6:c.778G>C
|
NP_000448.3:p.Glu260Gln
|
|
NM_001287183.2:c.703G>C
|
NP_001274112.1:p.Glu235Gln
|
|
NM_175914.5:c.712G>C
MANE Select
|
NP_787110.2:p.Glu238Gln
|
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