ENST00000456935.7:c.762T>A
MANE Select
|
ENSP00000395473.2:p.Thr254=
|
|
ENST00000221363.8:c.762T>A
|
ENSP00000221363.4:p.Thr254=
|
|
ENST00000456935.6:c.762T>A
|
ENSP00000395473.2:p.Thr254=
|
|
ENST00000466794.5:n.744T>A
|
|
|
ENST00000486847.2:c.465T>A
|
ENSP00000470174.1:p.Thr155=
|
|
NM_000528.3:c.762T>A
|
NP_000519.2:p.Thr254=
|
|
NM_001173498.1:c.762T>A
|
NP_001166969.1:p.Thr254=
|
|
XM_005259913.1:c.762T>A
|
XP_005259970.1:p.Thr254=
|
|
XM_005259913.2:c.762T>A
|
XP_005259970.1:p.Thr254=
|
|
XM_024451518.1:c.-257T>A
|
XP_024307286.1:n.-257T>A
|
|
NM_000528.4:c.762T>A
MANE Select
|
NP_000519.2:p.Thr254=
|
|
NM_001173498.2:c.762T>A
|
NP_001166969.1:p.Thr254=
|
|