ENST00000699947.1:c.483C>T
|
ENSP00000514703.1:p.Gly161=
|
|
ENST00000699948.1:c.483C>T
|
ENSP00000514704.1:p.Gly161=
|
|
ENST00000699950.1:n.435C>T
|
|
|
ENST00000382745.9:c.483C>T
MANE Select
|
ENSP00000372193.4:p.Gly161=
|
|
ENST00000262318.12:c.411C>T
|
ENSP00000262318.8:p.Gly137=
|
|
ENST00000382745.8:c.483C>T
|
ENSP00000372193.4:p.Gly161=
|
|
ENST00000448525.5:c.411C>T
|
ENSP00000410907.1:p.Gly137=
|
|
ENST00000561665.5:n.513C>T
|
|
|
ENST00000567139.1:n.534C>T
|
|
|
ENST00000569851.6:c.309C>T
|
ENSP00000461009.1:p.Gly103=
|
|
NM_001114331.2:c.411C>T
|
NP_001107803.1:p.Gly137=
|
|
NM_001287.5:c.483C>T
|
NP_001278.1:p.Gly161=
|
|
XM_011522354.1:c.309C>T
|
XP_011520656.1:p.Gly103=
|
|
NM_001287.6:c.483C>T
MANE Select
|
NP_001278.1:p.Gly161=
|
|
NM_001114331.3:c.411C>T
|
NP_001107803.1:p.Gly137=
|
|