ENST00000695651.1:n.1005T>C
|
|
|
ENST00000695652.1:c.2534T>C
|
ENSP00000512083.1:p.Val845Ala
|
|
ENST00000695653.1:c.566T>C
|
ENSP00000512084.1:p.Val189Ala
|
|
ENST00000695654.1:c.1781T>C
|
ENSP00000512085.1:p.Val594Ala
|
|
ENST00000695655.1:c.1598T>C
|
ENSP00000512086.1:n.1598T>C
|
|
ENST00000695692.1:n.2021T>C
|
|
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ENST00000245907.11:c.2657T>C
MANE Select
|
ENSP00000245907.4:p.Val886Ala
|
|
ENST00000245907.10:c.2657T>C
|
ENSP00000245907.4:p.Val886Ala
|
|
ENST00000594005.1:n.233T>C
|
|
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NM_000064.3:c.2657T>C
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NP_000055.2:p.Val886Ala
|
|
NM_000064.4:c.2657T>C
MANE Select
|
NP_000055.2:p.Val886Ala
|
|