ENST00000383788.10:c.666G>C
MANE Select
|
ENSP00000373298.3:p.Gly222=
|
|
ENST00000604401.2:n.662G>C
|
|
|
ENST00000679838.1:c.*428G>C
|
ENSP00000505708.1:n.*428G>C
|
|
ENST00000680545.1:n.432G>C
|
|
|
ENST00000681097.1:c.666G>C
|
ENSP00000505397.1:p.Gly222=
|
|
ENST00000383781.8:c.636G>C
|
ENSP00000373291.3:p.Gly212=
|
|
ENST00000383786.9:c.564G>C
|
ENSP00000373296.3:p.Gly188=
|
|
ENST00000383788.9:c.666G>C
|
ENSP00000373298.3:p.Gly222=
|
|
ENST00000603808.5:c.666G>C
|
ENSP00000474271.1:p.Gly222=
|
|
ENST00000605797.1:c.495G>C
|
ENSP00000474936.1:p.Gly165=
|
|
NM_005677.3:c.666G>C
|
NP_005668.2:p.Gly222=
|
|
NM_080538.2:c.636G>C
|
NP_536799.1:p.Gly212=
|
|
NM_080539.3:c.564G>C
|
NP_536800.2:p.Gly188=
|
|
NM_005677.4:c.666G>C
MANE Select
|
NP_005668.2:p.Gly222=
|
|
NM_080539.4:c.564G>C
|
NP_536800.2:p.Gly188=
|
|