ENST00000698727.1:n.1573T>G
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|
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ENST00000698728.1:n.2092T>G
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|
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ENST00000698729.1:n.3638T>G
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|
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ENST00000698730.1:n.3638T>G
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|
|
ENST00000698731.1:c.2372T>G
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ENSP00000513898.1:p.Phe791Cys
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ENST00000698732.1:c.*1374T>G
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ENSP00000513899.1:n.*1374T>G
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ENST00000698733.1:c.*1700T>G
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ENSP00000513900.1:n.*1700T>G
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|
ENST00000698734.1:c.2513T>G
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ENSP00000513901.1:p.Phe838Cys
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ENST00000698735.1:n.2628T>G
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|
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ENST00000698736.1:n.2628T>G
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|
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ENST00000698737.1:n.2628T>G
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|
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ENST00000698738.1:n.2628T>G
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|
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ENST00000698739.1:n.2628T>G
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|
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ENST00000372371.8:c.2513T>G
MANE Select
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ENSP00000361446.3:p.Phe838Cys
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ENST00000372371.7:c.2513T>G
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ENSP00000361446.3:p.Phe838Cys
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|
ENST00000472014.5:n.469+4632T>G
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|
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NM_007055.3:c.2513T>G
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NP_008986.2:p.Phe838Cys
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|
NM_007055.4:c.2513T>G
MANE Select
|
NP_008986.2:p.Phe838Cys
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