ENST00000695651.1:n.1065G>T
|
|
|
ENST00000695652.1:c.2594G>T
|
ENSP00000512083.1:p.Gly865Val
|
|
ENST00000695653.1:c.626G>T
|
ENSP00000512084.1:p.Gly209Val
|
|
ENST00000695654.1:c.1841G>T
|
ENSP00000512085.1:p.Gly614Val
|
|
ENST00000695655.1:c.1658G>T
|
ENSP00000512086.1:n.1658G>T
|
|
ENST00000695692.1:n.2081G>T
|
|
|
ENST00000245907.11:c.2717G>T
MANE Select
|
ENSP00000245907.4:p.Gly906Val
|
|
ENST00000245907.10:c.2717G>T
|
ENSP00000245907.4:p.Gly906Val
|
|
ENST00000594005.1:n.293G>T
|
|
|
NM_000064.3:c.2717G>T
|
NP_000055.2:p.Gly906Val
|
|
NM_000064.4:c.2717G>T
MANE Select
|
NP_000055.2:p.Gly906Val
|
|