|
NM_001142800.2:c.8143C>T
(EYS)
MANE Select
|
NP_001136272.1:p.Arg2715Ter
|
|
ENST00000503581.6:c.8143C>T
(EYS)
MANE Select
|
ENSP00000424243.1:p.Arg2715Ter
|
|
NM_001142800.1:c.8143C>T
(EYS)
|
NP_001136272.1:p.Arg2715Ter
|
|
NM_001292009.1:c.8206C>T
(EYS)
|
NP_001278938.1:p.Arg2736Ter
|
|
NM_001292009.2:c.8206C>T
(EYS)
|
NP_001278938.1:p.Arg2736Ter
|
|
ENST00000370616.6:c.8206C>T
(EYS)
|
ENSP00000359650.2:p.Arg2736Ter
|
|
ENST00000370618.7:c.8143C>T
(EYS)
|
ENSP00000359652.4:p.Arg2715Ter
|
|
ENST00000370621.7:c.8206C>T
(EYS)
|
ENSP00000359655.3:p.Arg2736Ter
|
|
ENST00000503581.5:c.8143C>T
(EYS)
|
ENSP00000424243.1:p.Arg2715Ter
|
|
ENST00000505138.1:c.363+15247G>A
(PHF3)
|
|