ENST00000261024.7:c.206C>T
MANE Select
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ENSP00000261024.3:p.Ala69Val
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ENST00000261024.6:c.206C>T
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ENSP00000261024.2:p.Ala69Val
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ENST00000418714.1:n.647C>T
|
|
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ENST00000427241.5:c.206C>T
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ENSP00000390005.1:p.Ala69Val
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ENST00000479598.5:n.487C>T
|
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NM_014585.5:c.206C>T , LRG_837t1:c.206C>T
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NP_055400.1:p.Ala69Val
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XM_005246505.1:c.86C>T
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XP_005246562.1:p.Ala29Val
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XM_005246505.2:c.86C>T
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XP_005246562.1:p.Ala29Val
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XM_017003938.2:c.86C>T
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XP_016859427.1:p.Ala29Val
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NM_014585.6:c.206C>T
MANE Select
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NP_055400.1:p.Ala69Val
|
|