|
NM_002506.3:c.477G>A
(NGF)
MANE Select
|
NP_002497.2:p.Val159=
|
|
ENST00000369512.3:c.477G>A
(NGF)
MANE Select
|
ENSP00000358525.2:p.Val159=
|
|
NM_002506.2:c.477G>A , LRG_260t1:c.477G>A
(NGF)
|
NP_002497.2:p.Val159=
|
|
NR_157569.1:n.207+3079C>T
(NGF-AS1)
|
|
|
ENST00000369512.2:c.477G>A
(NGF)
|
ENSP00000358525.2:p.Val159=
|
|
ENST00000675637.2:c.477G>A
(NGF)
|
ENSP00000502831.1:p.Val159=
|
|
ENST00000676038.2:c.477G>A
(NGF)
|
ENSP00000502380.1:p.Val159=
|
|
ENST00000679806.1:c.477G>A
(NGF)
|
ENSP00000506492.1:p.Val159=
|
|
ENST00000680116.1:c.477G>A
(NGF)
|
ENSP00000505694.1:p.Val159=
|
|
ENST00000680540.1:c.477G>A
(NGF)
|
ENSP00000506569.1:p.Val159=
|
|
ENST00000680752.1:c.477G>A
(NGF)
|
ENSP00000505558.1:p.Val159=
|
|
ENST00000681124.1:c.6G>A
(NGF)
|
ENSP00000506364.1:p.Val2=
|
|
XM_006710663.2:c.477G>A
(NGF)
|
XP_006710726.1:p.Val159=
|
|
XM_006710663.3:c.477G>A
(NGF)
|
XP_006710726.1:p.Val159=
|
|
XM_006710665.2:c.477G>A
(NGF)
|
XP_006710728.1:p.Val159=
|
|
XM_011541518.1:c.642G>A
(NGF)
|
XP_011539820.1:p.Val214=
|
|
XM_011541518.2:c.642G>A
(NGF)
|
XP_011539820.1:p.Val214=
|
