ENST00000225964.10:c.1434T>A
MANE Select
|
ENSP00000225964.6:p.Thr478=
|
|
ENST00000225964.9:c.1434T>A
|
ENSP00000225964.5:p.Thr478=
|
|
ENST00000471344.1:n.378T>A
|
|
|
NM_000088.3:c.1434T>A , LRG_1t1:c.1434T>A
|
NP_000079.2:p.Thr478=
|
|
XM_005257058.3:c.1434T>A
|
XP_005257115.2:p.Thr478=
|
|
XM_005257059.3:c.957+1566T>A
|
XP_005257116.2:n.957+1566T>A
|
|
XM_011524341.1:c.1236T>A
|
XP_011522643.1:p.Thr412=
|
|
XM_005257058.4:c.1434T>A
|
XP_005257115.2:p.Thr478=
|
|
XM_005257059.4:c.957+1566T>A
|
XP_005257116.2:n.957+1566T>A
|
|
NM_000088.4:c.1434T>A
MANE Select
|
NP_000079.2:p.Thr478=
|
|