|
NM_001346754.2:c.699A>T
(PIGW)
MANE Select
|
NP_001333683.1:p.Gly233=
|
|
ENST00000614443.2:c.699A>T
(PIGW)
MANE Select
|
ENSP00000482202.1:p.Gly233=
|
|
NM_001346754.1:c.699A>T
(PIGW)
|
NP_001333683.1:p.Gly233=
|
|
NM_001346755.1:c.699A>T
(PIGW)
|
NP_001333684.1:p.Gly233=
|
|
NM_001346755.2:c.699A>T
(PIGW)
|
NP_001333684.1:p.Gly233=
|
|
NM_178517.3:c.699A>T
(PIGW)
|
NP_848612.2:p.Gly233=
|
|
NM_178517.4:c.699A>T
(PIGW)
|
NP_848612.2:p.Gly233=
|
|
NM_178517.5:c.699A>T
(PIGW)
|
NP_848612.2:p.Gly233=
|
|
ENST00000610496.1:n.396-3696T>A
(MYO19)
|
|
|
ENST00000614443.1:c.699A>T
(PIGW)
|
ENSP00000482202.1:p.Gly233=
|
|
ENST00000617167.1:n.164-2167T>A
(MYO19)
|
|
|
ENST00000619326.1:c.699A>T
(PIGW)
|
ENSP00000480475.1:p.Gly233=
|
|
ENST00000620233.1:c.699A>T
(PIGW)
|
ENSP00000480021.1:p.Gly233=
|
|
XM_005257238.1:c.699A>T
(PIGW)
|
XP_005257295.1:p.Gly233=
|
|
XM_011524646.1:c.699A>T
(PIGW)
|
XP_011522948.1:p.Gly233=
|
