ENST00000461280.2:n.657T>A
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ENST00000684116.1:n.252T>A
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ENST00000684241.1:n.2192T>A
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ENST00000262186.10:c.1359T>A
MANE Select
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ENSP00000262186.5:p.Ala453=
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ENST00000330883.9:c.339T>A
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ENSP00000328531.4:p.Ala113=
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ENST00000262186.9:c.1359T>A
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ENSP00000262186.5:p.Ala453=
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ENST00000330883.8:c.339T>A
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ENSP00000328531.4:p.Ala113=
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ENST00000430723.4:c.1011T>A
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ENSP00000387657.4:p.Ala337=
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ENST00000461280.1:n.646T>A
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ENST00000473610.5:n.664T>A
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ENST00000532957.5:n.1582T>A
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NM_000238.3:c.1359T>A , LRG_288t1:c.1359T>A
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NP_000229.1:p.Ala453=
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NM_001204798.1:c.339T>A
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NP_001191727.1:p.Ala113=
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NM_172056.2:c.1359T>A , LRG_288t2:c.1359T>A
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NP_742053.1:p.Ala453=
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NM_172057.2:c.339T>A , LRG_288t3:c.339T>A
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NP_742054.1:p.Ala113=
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XM_011516185.1:c.1059T>A
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XP_011514487.1:p.Ala353=
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XM_011516186.1:c.1359T>A
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XP_011514488.1:p.Ala453=
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XM_011516185.2:c.1059T>A
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XP_011514487.1:p.Ala353=
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XM_011516186.3:c.1359T>A
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XP_011514488.1:p.Ala453=
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XM_017012195.1:c.1209T>A
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XP_016867684.1:p.Ala403=
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XM_017012196.1:c.1182T>A
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XP_016867685.1:p.Ala394=
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NM_000238.4:c.1359T>A
MANE Select
|
NP_000229.1:p.Ala453=
|
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NM_001204798.2:c.339T>A
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NP_001191727.1:p.Ala113=
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NM_172057.3:c.339T>A
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NP_742054.1:p.Ala113=
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