ENST00000220420.10:c.630A>G
MANE Select
|
ENSP00000220420.5:p.Thr210=
|
|
ENST00000635871.1:n.99A>G
|
|
|
ENST00000220420.9:c.630A>G
|
ENSP00000220420.5:p.Thr210=
|
|
ENST00000349114.8:c.384A>G
|
ENSP00000220419.8:p.Thr128=
|
|
ENST00000610827.4:c.627A>G
|
ENSP00000479732.1:p.Thr209=
|
|
ENST00000611276.4:c.381A>G
|
ENSP00000482542.1:p.Thr127=
|
|
ENST00000622115.1:c.633A>G
|
ENSP00000479638.1:p.Thr211=
|
|
NM_004245.3:c.384A>G
|
NP_004236.1:p.Thr128=
|
|
NM_201631.3:c.630A>G
|
NP_963925.2:p.Thr210=
|
|
XM_011522229.1:c.630A>G
|
XP_011520531.1:p.Thr210=
|
|
XR_931948.1:n.804A>G
|
|
|
NM_004245.4:c.384A>G
|
NP_004236.1:p.Thr128=
|
|
NM_201631.4:c.630A>G
MANE Select
|
NP_963925.2:p.Thr210=
|
|