ENST00000695651.1:n.1144G>T
|
|
|
ENST00000695652.1:c.2673G>T
|
ENSP00000512083.1:p.Val891=
|
|
ENST00000695653.1:c.705G>T
|
ENSP00000512084.1:p.Val235=
|
|
ENST00000695654.1:c.1920G>T
|
ENSP00000512085.1:p.Val640=
|
|
ENST00000695655.1:c.1737G>T
|
ENSP00000512086.1:n.1737G>T
|
|
ENST00000695692.1:n.2160G>T
|
|
|
ENST00000245907.11:c.2796G>T
MANE Select
|
ENSP00000245907.4:p.Val932=
|
|
ENST00000245907.10:c.2796G>T
|
ENSP00000245907.4:p.Val932=
|
|
ENST00000594005.1:n.372G>T
|
|
|
NM_000064.3:c.2796G>T
|
NP_000055.2:p.Val932=
|
|
NM_000064.4:c.2796G>T
MANE Select
|
NP_000055.2:p.Val932=
|
|