ENST00000695651.1:n.1095T>C
|
|
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ENST00000695652.1:c.2624T>C
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ENSP00000512083.1:p.Val875Ala
|
|
ENST00000695653.1:c.656T>C
|
ENSP00000512084.1:p.Val219Ala
|
|
ENST00000695654.1:c.1871T>C
|
ENSP00000512085.1:p.Val624Ala
|
|
ENST00000695655.1:c.1688T>C
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ENSP00000512086.1:n.1688T>C
|
|
ENST00000695692.1:n.2111T>C
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|
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ENST00000245907.11:c.2747T>C
MANE Select
|
ENSP00000245907.4:p.Val916Ala
|
|
ENST00000245907.10:c.2747T>C
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ENSP00000245907.4:p.Val916Ala
|
|
ENST00000594005.1:n.323T>C
|
|
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NM_000064.3:c.2747T>C
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NP_000055.2:p.Val916Ala
|
|
NM_000064.4:c.2747T>C
MANE Select
|
NP_000055.2:p.Val916Ala
|
|