ENST00000692443.1:c.248T>A
MANE Select
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ENSP00000509163.1:p.Phe83Tyr
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ENST00000419277.5:c.248T>A
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ENSP00000393566.1:p.Phe83Tyr
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ENST00000453337.1:c.248T>A
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ENSP00000390929.1:p.Phe83Tyr
|
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ENST00000463066.1:n.343T>A
|
|
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ENST00000476642.5:n.224T>A
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|
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ENST00000479107.1:n.293T>A
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|
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NM_001242524.1:c.248T>A
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NP_001229453.1:p.Phe83Tyr
|
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NM_001242525.1:c.248T>A
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NP_001229454.1:p.Phe83Tyr
|
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NM_033554.3:c.248T>A
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NP_291032.2:p.Phe83Tyr
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XM_011514559.1:c.248T>A
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XP_011512861.1:p.Phe83Tyr
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NM_001242524.2:c.248T>A
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NP_001229453.1:p.Phe83Tyr
|
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NM_001242525.2:c.248T>A
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NP_001229454.1:p.Phe83Tyr
|
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