ENST00000695651.1:n.798T>C
|
|
|
ENST00000695652.1:c.2327T>C
|
ENSP00000512083.1:p.Val776Ala
|
|
ENST00000695653.1:c.359T>C
|
ENSP00000512084.1:p.Val120Ala
|
|
ENST00000695654.1:c.1574T>C
|
ENSP00000512085.1:p.Val525Ala
|
|
ENST00000695655.1:c.1391T>C
|
ENSP00000512086.1:n.1391T>C
|
|
ENST00000695692.1:n.1814T>C
|
|
|
ENST00000245907.11:c.2450T>C
MANE Select
|
ENSP00000245907.4:p.Val817Ala
|
|
ENST00000245907.10:c.2450T>C
|
ENSP00000245907.4:p.Val817Ala
|
|
ENST00000602053.1:n.498T>C
|
|
|
NM_000064.3:c.2450T>C
|
NP_000055.2:p.Val817Ala
|
|
NM_000064.4:c.2450T>C
MANE Select
|
NP_000055.2:p.Val817Ala
|
|