ENST00000695651.1:n.897T>C
|
|
|
ENST00000695652.1:c.2426T>C
|
ENSP00000512083.1:p.Val809Ala
|
|
ENST00000695653.1:c.458T>C
|
ENSP00000512084.1:p.Val153Ala
|
|
ENST00000695654.1:c.1673T>C
|
ENSP00000512085.1:p.Val558Ala
|
|
ENST00000695655.1:c.1490T>C
|
ENSP00000512086.1:n.1490T>C
|
|
ENST00000695692.1:n.1913T>C
|
|
|
ENST00000245907.11:c.2549T>C
MANE Select
|
ENSP00000245907.4:p.Val850Ala
|
|
ENST00000245907.10:c.2549T>C
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ENSP00000245907.4:p.Val850Ala
|
|
ENST00000594005.1:n.30T>C
|
|
|
ENST00000602053.1:n.597T>C
|
|
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NM_000064.3:c.2549T>C
|
NP_000055.2:p.Val850Ala
|
|
NM_000064.4:c.2549T>C
MANE Select
|
NP_000055.2:p.Val850Ala
|
|