ENST00000553106.6:c.984T>G
MANE Select
|
ENSP00000448059.1:p.Thr328=
|
|
ENST00000307000.7:c.969T>G
|
ENSP00000303500.2:p.Thr323=
|
|
ENST00000549247.6:n.743T>G
|
|
|
ENST00000551114.2:n.646T>G
|
|
|
ENST00000553106.5:c.984T>G
|
ENSP00000448059.1:p.Thr328=
|
|
ENST00000635477.1:c.88T>G
|
|
|
ENST00000635528.1:n.499T>G
|
|
|
NM_000277.1:c.984T>G
|
NP_000268.1:p.Thr328=
|
|
XM_011538422.1:c.927T>G
|
XP_011536724.1:p.Thr309=
|
|
NM_000277.2:c.984T>G
|
NP_000268.1:p.Thr328=
|
|
NM_001354304.1:c.984T>G
|
NP_001341233.1:p.Thr328=
|
|
NM_000277.3:c.984T>G
MANE Select
|
NP_000268.1:p.Thr328=
|
|
NM_001354304.2:c.984T>G
|
NP_001341233.1:p.Thr328=
|
|