ENST00000695651.1:n.857T=
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|
|
ENST00000695652.1:c.2386T=
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ENSP00000512083.1:p.Tyr796=
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|
ENST00000695653.1:c.418T=
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ENSP00000512084.1:p.Tyr140=
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ENST00000695654.1:c.1633T=
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ENSP00000512085.1:p.Tyr545=
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ENST00000695655.1:c.1450T=
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ENSP00000512086.1:n.1450T=
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|
ENST00000695692.1:n.1873T=
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|
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ENST00000245907.11:c.2509T=
MANE Select
|
ENSP00000245907.4:p.Tyr837=
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ENST00000245907.10:c.2509T=
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ENSP00000245907.4:p.Tyr837=
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|
ENST00000602053.1:n.557T=
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NM_000064.3:c.2509T=
|
NP_000055.2:p.Tyr837=
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|
NM_000064.4:c.2509T=
MANE Select
|
NP_000055.2:p.Tyr837=
|
|