ENST00000402696.9:c.866C>T
MANE Select
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ENSP00000385834.3:p.Ala289Val
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ENST00000402696.7:c.866C>T
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ENSP00000385834.3:p.Ala289Val
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ENST00000485977.1:c.231C>T
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ENSP00000418716.1:p.Gly77=
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NM_001063.3:c.866C>T
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NP_001054.1:p.Ala289Val
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XM_011513100.1:c.866C>T
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XP_011511402.1:p.Ala289Val
|
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NM_001354703.1:c.734C>T
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NP_001341632.1:p.Ala245Val
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NM_001354704.1:c.485C>T
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NP_001341633.1:p.Ala162Val
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NM_001063.4:c.866C>T
MANE Select
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NP_001054.2:p.Ala289Val
|
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NM_001354703.2:c.734C>T
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NP_001341632.2:p.Ala245Val
|
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NM_001354704.2:c.485C>T
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NP_001341633.2:p.Ala162Val
|
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