ENST00000461280.2:n.433T>G
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ENST00000684116.1:n.28T>G
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ENST00000684241.1:n.1968T>G
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ENST00000262186.10:c.1135T>G
MANE Select
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ENSP00000262186.5:p.Ser379Ala
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ENST00000330883.9:c.115T>G
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ENSP00000328531.4:p.Ser39Ala
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ENST00000262186.9:c.1135T>G
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ENSP00000262186.5:p.Ser379Ala
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ENST00000330883.8:c.115T>G
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ENSP00000328531.4:p.Ser39Ala
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ENST00000430723.4:c.787T>G
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ENSP00000387657.4:p.Ser263Ala
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ENST00000461280.1:n.422T>G
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ENST00000473610.5:n.440T>G
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ENST00000532957.5:n.1358T>G
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NM_000238.3:c.1135T>G , LRG_288t1:c.1135T>G
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NP_000229.1:p.Ser379Ala
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NM_001204798.1:c.115T>G
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NP_001191727.1:p.Ser39Ala
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NM_172056.2:c.1135T>G , LRG_288t2:c.1135T>G
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NP_742053.1:p.Ser379Ala
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NM_172057.2:c.115T>G , LRG_288t3:c.115T>G
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NP_742054.1:p.Ser39Ala
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XM_011516185.1:c.835T>G
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XP_011514487.1:p.Ser279Ala
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XM_011516186.1:c.1135T>G
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XP_011514488.1:p.Ser379Ala
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XM_011516185.2:c.835T>G
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XP_011514487.1:p.Ser279Ala
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XM_011516186.3:c.1135T>G
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XP_011514488.1:p.Ser379Ala
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XM_017012195.1:c.985T>G
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XP_016867684.1:p.Ser329Ala
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XM_017012196.1:c.958T>G
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XP_016867685.1:p.Ser320Ala
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NM_000238.4:c.1135T>G
MANE Select
|
NP_000229.1:p.Ser379Ala
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NM_001204798.2:c.115T>G
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NP_001191727.1:p.Ser39Ala
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NM_172057.3:c.115T>G
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NP_742054.1:p.Ser39Ala
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