ENST00000695651.1:n.1142G=
|
|
|
ENST00000695652.1:c.2671G=
|
ENSP00000512083.1:p.Val891=
|
|
ENST00000695653.1:c.703G=
|
ENSP00000512084.1:p.Val235=
|
|
ENST00000695654.1:c.1918G=
|
ENSP00000512085.1:p.Val640=
|
|
ENST00000695655.1:c.1735G=
|
ENSP00000512086.1:n.1735G=
|
|
ENST00000695692.1:n.2158G=
|
|
|
ENST00000245907.11:c.2794G=
MANE Select
|
ENSP00000245907.4:p.Val932=
|
|
ENST00000245907.10:c.2794G=
|
ENSP00000245907.4:p.Val932=
|
|
ENST00000594005.1:n.370G=
|
|
|
NM_000064.3:c.2794G=
|
NP_000055.2:p.Val932=
|
|
NM_000064.4:c.2794G=
MANE Select
|
NP_000055.2:p.Val932=
|
|