ENST00000695651.1:n.1050T>C
|
|
|
ENST00000695652.1:c.2579T>C
|
ENSP00000512083.1:p.Val860Ala
|
|
ENST00000695653.1:c.611T>C
|
ENSP00000512084.1:p.Val204Ala
|
|
ENST00000695654.1:c.1826T>C
|
ENSP00000512085.1:p.Val609Ala
|
|
ENST00000695655.1:c.1643T>C
|
ENSP00000512086.1:n.1643T>C
|
|
ENST00000695692.1:n.2066T>C
|
|
|
ENST00000245907.11:c.2702T>C
MANE Select
|
ENSP00000245907.4:p.Val901Ala
|
|
ENST00000245907.10:c.2702T>C
|
ENSP00000245907.4:p.Val901Ala
|
|
ENST00000594005.1:n.278T>C
|
|
|
NM_000064.3:c.2702T>C
|
NP_000055.2:p.Val901Ala
|
|
NM_000064.4:c.2702T>C
MANE Select
|
NP_000055.2:p.Val901Ala
|
|