ENST00000461280.2:n.1175G>C
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ENST00000683359.1:n.1G>C
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ENST00000684241.1:n.2710G>C
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ENST00000262186.10:c.1877G>C
MANE Select
|
ENSP00000262186.5:p.Gly626Ala
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ENST00000330883.9:c.857G>C
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ENSP00000328531.4:p.Gly286Ala
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ENST00000262186.9:c.1877G>C
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ENSP00000262186.5:p.Gly626Ala
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ENST00000330883.8:c.857G>C
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ENSP00000328531.4:p.Gly286Ala
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ENST00000430723.4:c.1529G>C
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ENSP00000387657.4:p.Gly510Ala
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ENST00000461280.1:n.1164G>C
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ENST00000473610.5:n.1182G>C
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ENST00000532957.5:n.2100G>C
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NM_000238.3:c.1877G>C , LRG_288t1:c.1877G>C
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NP_000229.1:p.Gly626Ala
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NM_001204798.1:c.857G>C
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NP_001191727.1:p.Gly286Ala
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NM_172056.2:c.1877G>C , LRG_288t2:c.1877G>C
|
NP_742053.1:p.Gly626Ala
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NM_172057.2:c.857G>C , LRG_288t3:c.857G>C
|
NP_742054.1:p.Gly286Ala
|
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XM_011516185.1:c.1577G>C
|
XP_011514487.1:p.Gly526Ala
|
|
XM_011516186.1:c.1877G>C
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XP_011514488.1:p.Gly626Ala
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XM_011516185.2:c.1577G>C
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XP_011514487.1:p.Gly526Ala
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XM_011516186.3:c.1877G>C
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XP_011514488.1:p.Gly626Ala
|
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XM_017012195.1:c.1727G>C
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XP_016867684.1:p.Gly576Ala
|
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XM_017012196.1:c.1700G>C
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XP_016867685.1:p.Gly567Ala
|
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NM_000238.4:c.1877G>C
MANE Select
|
NP_000229.1:p.Gly626Ala
|
|
NM_001204798.2:c.857G>C
|
NP_001191727.1:p.Gly286Ala
|
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NM_172057.3:c.857G>C
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NP_742054.1:p.Gly286Ala
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