ENST00000461280.2:n.656C>T
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ENST00000684116.1:n.251C>T
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|
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ENST00000684241.1:n.2191C>T
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ENST00000262186.10:c.1358C>T
MANE Select
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ENSP00000262186.5:p.Ala453Val
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ENST00000330883.9:c.338C>T
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ENSP00000328531.4:p.Ala113Val
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ENST00000262186.9:c.1358C>T
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ENSP00000262186.5:p.Ala453Val
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ENST00000330883.8:c.338C>T
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ENSP00000328531.4:p.Ala113Val
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ENST00000430723.4:c.1010C>T
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ENSP00000387657.4:p.Ala337Val
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ENST00000461280.1:n.645C>T
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ENST00000473610.5:n.663C>T
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ENST00000532957.5:n.1581C>T
|
|
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NM_000238.3:c.1358C>T , LRG_288t1:c.1358C>T
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NP_000229.1:p.Ala453Val
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NM_001204798.1:c.338C>T
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NP_001191727.1:p.Ala113Val
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NM_172056.2:c.1358C>T , LRG_288t2:c.1358C>T
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NP_742053.1:p.Ala453Val
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NM_172057.2:c.338C>T , LRG_288t3:c.338C>T
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NP_742054.1:p.Ala113Val
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XM_011516185.1:c.1058C>T
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XP_011514487.1:p.Ala353Val
|
|
XM_011516186.1:c.1358C>T
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XP_011514488.1:p.Ala453Val
|
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XM_011516185.2:c.1058C>T
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XP_011514487.1:p.Ala353Val
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XM_011516186.3:c.1358C>T
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XP_011514488.1:p.Ala453Val
|
|
XM_017012195.1:c.1208C>T
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XP_016867684.1:p.Ala403Val
|
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XM_017012196.1:c.1181C>T
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XP_016867685.1:p.Ala394Val
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NM_000238.4:c.1358C>T
MANE Select
|
NP_000229.1:p.Ala453Val
|
|
NM_001204798.2:c.338C>T
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NP_001191727.1:p.Ala113Val
|
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NM_172057.3:c.338C>T
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NP_742054.1:p.Ala113Val
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