ENST00000377047.9:c.666C>T
(GPC6)
MANE Select
|
ENSP00000366246.3:p.Val222=
|
|
ENST00000377047.8:c.666C>T
(GPC6)
|
ENSP00000366246.3:p.Val222=
|
|
NM_005708.3:c.666C>T
(GPC6)
|
NP_005699.1:p.Val222=
|
|
NR_046536.1:n.380+316G>A
(GPC6-AS2)
|
|
|
XM_011521044.1:c.456C>T
(GPC6)
|
XP_011519346.1:p.Val152=
|
|
NM_005708.4:c.666C>T
(GPC6)
|
NP_005699.1:p.Val222=
|
|
XM_011521044.2:c.456C>T
(GPC6)
|
XP_011519346.1:p.Val152=
|
|
XM_017020298.1:c.456C>T
(GPC6)
|
XP_016875787.1:p.Val152=
|
|
XM_017020299.2:c.456C>T
(GPC6)
|
XP_016875788.1:p.Val152=
|
|
XM_017020300.1:c.456C>T
(GPC6)
|
XP_016875789.1:p.Val152=
|
|
XM_017020301.1:c.300C>T
(GPC6)
|
XP_016875790.1:p.Val100=
|
|
NM_005708.5:c.666C>T
(GPC6)
MANE Select
|
NP_005699.1:p.Val222=
|
|