ENST00000383788.10:c.771T>G
MANE Select
|
ENSP00000373298.3:p.Ser257=
|
|
ENST00000604401.2:n.767T>G
|
|
|
ENST00000679838.1:c.*533T>G
|
ENSP00000505708.1:n.*533T>G
|
|
ENST00000680545.1:n.537T>G
|
|
|
ENST00000681097.1:c.771T>G
|
ENSP00000505397.1:p.Ser257=
|
|
ENST00000383781.8:c.741T>G
|
ENSP00000373291.3:p.Ser247=
|
|
ENST00000383786.9:c.669T>G
|
ENSP00000373296.3:p.Ser223=
|
|
ENST00000383788.9:c.771T>G
|
ENSP00000373298.3:p.Ser257=
|
|
ENST00000603808.5:c.771T>G
|
ENSP00000474271.1:p.Ser257=
|
|
NM_005677.3:c.771T>G
|
NP_005668.2:p.Ser257=
|
|
NM_080538.2:c.741T>G
|
NP_536799.1:p.Ser247=
|
|
NM_080539.3:c.669T>G
|
NP_536800.2:p.Ser223=
|
|
NM_005677.4:c.771T>G
MANE Select
|
NP_005668.2:p.Ser257=
|
|
NM_080539.4:c.669T>G
|
NP_536800.2:p.Ser223=
|
|