ENST00000695651.1:n.795G>T
|
|
|
ENST00000695652.1:c.2324G>T
|
ENSP00000512083.1:p.Cys775Phe
|
|
ENST00000695653.1:c.356G>T
|
ENSP00000512084.1:p.Cys119Phe
|
|
ENST00000695654.1:c.1571G>T
|
ENSP00000512085.1:p.Cys524Phe
|
|
ENST00000695655.1:c.1388G>T
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ENSP00000512086.1:n.1388G>T
|
|
ENST00000695692.1:n.1811G>T
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|
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ENST00000245907.11:c.2447G>T
MANE Select
|
ENSP00000245907.4:p.Cys816Phe
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ENST00000245907.10:c.2447G>T
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ENSP00000245907.4:p.Cys816Phe
|
|
ENST00000602053.1:n.495G>T
|
|
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NM_000064.3:c.2447G>T
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NP_000055.2:p.Cys816Phe
|
|
NM_000064.4:c.2447G>T
MANE Select
|
NP_000055.2:p.Cys816Phe
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