ENST00000262043.8:c.*7641G=
(PHF3)
MANE Select
|
ENSP00000262043.4:n.*7641G=
|
|
ENST00000503581.6:c.8682C=
(EYS)
MANE Select
|
ENSP00000424243.1:p.Gly2894=
|
|
ENST00000370616.6:c.8745C=
(EYS)
|
ENSP00000359650.2:p.Gly2915=
|
|
ENST00000370618.7:c.8682C=
(EYS)
|
ENSP00000359652.4:p.Gly2894=
|
|
ENST00000370621.7:c.8745C=
(EYS)
|
ENSP00000359655.3:p.Gly2915=
|
|
ENST00000503581.5:c.8682C=
(EYS)
|
ENSP00000424243.1:p.Gly2894=
|
|
ENST00000505138.1:c.363+9987G=
(PHF3)
|
|
|
NM_001142800.1:c.8682C=
(EYS)
|
NP_001136272.1:p.Gly2894=
|
|
NM_001292009.1:c.8745C=
(EYS)
|
NP_001278938.1:p.Gly2915=
|
|
NM_001142800.2:c.8682C=
(EYS)
MANE Select
|
NP_001136272.1:p.Gly2894=
|
|
NM_001290259.2:c.*7641G=
(PHF3)
|
NP_001277188.1:n.*7641G=
|
|
NM_001370348.2:c.*7641G=
(PHF3)
MANE Select
|
NP_001357277.1:n.*7641G=
|
|
NM_001370349.2:c.*7641G=
(PHF3)
|
NP_001357278.1:n.*7641G=
|
|
NM_001370350.2:c.*7641G=
(PHF3)
|
NP_001357279.1:n.*7641G=
|
|
NM_015153.4:c.*7641G=
(PHF3)
|
NP_055968.1:n.*7641G=
|
|
NM_001292009.2:c.8745C=
(EYS)
|
NP_001278938.1:p.Gly2915=
|
|