ENST00000225964.10:c.1458G>A
MANE Select
|
ENSP00000225964.6:p.Glu486=
|
|
ENST00000225964.9:c.1458G>A
|
ENSP00000225964.5:p.Glu486=
|
|
ENST00000471344.1:n.402G>A
|
|
|
NM_000088.3:c.1458G>A , LRG_1t1:c.1458G>A
|
NP_000079.2:p.Glu486=
|
|
XM_005257058.3:c.1458G>A
|
XP_005257115.2:p.Glu486=
|
|
XM_005257059.3:c.957+1590G>A
|
XP_005257116.2:n.957+1590G>A
|
|
XM_011524341.1:c.1260G>A
|
XP_011522643.1:p.Glu420=
|
|
XM_005257058.4:c.1458G>A
|
XP_005257115.2:p.Glu486=
|
|
XM_005257059.4:c.957+1590G>A
|
XP_005257116.2:n.957+1590G>A
|
|
NM_000088.4:c.1458G>A
MANE Select
|
NP_000079.2:p.Glu486=
|
|