ENST00000695651.1:n.790G>T
|
|
|
ENST00000695652.1:c.2319G>T
|
ENSP00000512083.1:p.Gly773=
|
|
ENST00000695653.1:c.351G>T
|
ENSP00000512084.1:p.Gly117=
|
|
ENST00000695654.1:c.1566G>T
|
ENSP00000512085.1:p.Gly522=
|
|
ENST00000695655.1:c.1383G>T
|
ENSP00000512086.1:n.1383G>T
|
|
ENST00000695692.1:n.1806G>T
|
|
|
ENST00000245907.11:c.2442G>T
MANE Select
|
ENSP00000245907.4:p.Gly814=
|
|
ENST00000245907.10:c.2442G>T
|
ENSP00000245907.4:p.Gly814=
|
|
ENST00000602053.1:n.490G>T
|
|
|
NM_000064.3:c.2442G>T
|
NP_000055.2:p.Gly814=
|
|
NM_000064.4:c.2442G>T
MANE Select
|
NP_000055.2:p.Gly814=
|
|