ENST00000684241.1:n.1301C>G
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ENST00000262186.10:c.468C>G
MANE Select
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ENSP00000262186.5:p.Ala156=
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ENST00000262186.9:c.468C>G
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ENSP00000262186.5:p.Ala156=
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ENST00000430723.4:c.234+57C>G
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ENSP00000387657.4:n.234+57C>G
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ENST00000532957.5:n.691C>G
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NM_000238.3:c.468C>G , LRG_288t1:c.468C>G
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NP_000229.1:p.Ala156=
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NM_172056.2:c.468C>G , LRG_288t2:c.468C>G
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NP_742053.1:p.Ala156=
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XM_011516185.1:c.168C>G
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XP_011514487.1:p.Ala56=
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XM_011516186.1:c.468C>G
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XP_011514488.1:p.Ala156=
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XM_011516185.2:c.168C>G
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XP_011514487.1:p.Ala56=
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XM_011516186.3:c.468C>G
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XP_011514488.1:p.Ala156=
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XM_017012195.1:c.318C>G
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XP_016867684.1:p.Ala106=
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XM_017012196.1:c.291C>G
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XP_016867685.1:p.Ala97=
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NM_000238.4:c.468C>G
MANE Select
|
NP_000229.1:p.Ala156=
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