|
ENST00000685515.1:c.-46G>T
(GORAB)
|
ENSP00000509073.1:n.-46G>T
|
|
|
ENST00000685976.1:n.166+194G>T
(GORAB)
|
|
|
|
ENST00000686135.1:n.48G>T
(GORAB)
|
|
|
|
ENST00000686870.1:c.-46G>T
(GORAB)
|
ENSP00000510121.1:n.-46G>T
|
|
|
ENST00000687370.1:n.13G>T
(GORAB)
|
|
|
|
ENST00000687880.1:c.-46G>T
(GORAB)
|
ENSP00000508486.1:n.-46G>T
|
|
|
ENST00000688499.1:c.-46G>T
(GORAB)
|
ENSP00000509581.1:n.-46G>T
|
|
|
ENST00000688688.1:c.-46G>T
(GORAB)
|
ENSP00000510426.1:n.-46G>T
|
|
|
ENST00000689173.1:c.-46G>T
(GORAB)
|
ENSP00000509341.1:n.-46G>T
|
|
|
ENST00000690124.1:n.7G>T
(GORAB)
|
|
|
|
ENST00000690898.1:n.32G>T
(GORAB)
|
|
|
|
ENST00000691235.1:n.32G>T
(GORAB)
|
|
|
|
ENST00000692234.1:c.-46G>T
(GORAB)
|
ENSP00000508508.1:n.-46G>T
|
|
|
ENST00000692875.1:c.-46G>T
(GORAB)
|
ENSP00000508785.1:n.-46G>T
|
|
|
ENST00000693173.1:c.-46G>T
(GORAB)
|
ENSP00000510143.1:n.-46G>T
|
|
|
ENST00000367762.2:c.-46G>T
(GORAB)
|
ENSP00000356736.2:n.-46G>T
|
|
|
ENST00000367763.8:c.-46G>T
(GORAB)
MANE Select
|
ENSP00000356737.4:n.-46G>T
|
|
|
ENST00000498166.6:c.-46G>T
(GORAB)
|
ENSP00000473336.2:n.-46G>T
|
|
|
ENST00000367762.1:c.30G>T
(GORAB)
|
ENSP00000356736.1:p.Ala10=
|
|
|
ENST00000367763.7:c.30G>T
(GORAB)
|
ENSP00000356737.3:p.Ala10=
|
|
|
ENST00000498166.5:c.28G>T
(GORAB)
|
|
|
|
NM_001146039.1:c.30G>T
(GORAB)
|
NP_001139511.1:p.Ala10=
|
|
|
NM_152281.2:c.30G>T
(GORAB)
|
NP_689494.2:p.Ala10=
|
|
|
NR_027397.1:n.57G>T
(GORAB)
|
|
|
|
NR_125958.1:n.162+270C>A
(GORAB-AS1)
|
|
|
|
XM_011510149.1:c.30G>T
(GORAB)
|
XP_011508451.1:p.Ala10=
|
|
|
XM_011510150.1:c.-703G>T
(GORAB)
|
XP_011508452.1:n.-703G>T
|
|
|
XM_011510151.1:c.-464G>T
(GORAB)
|
XP_011508453.1:n.-464G>T
|
|
|
NM_001320252.1:c.-811G>T
(GORAB)
|
NP_001307181.1:n.-811G>T
|
|
|
XM_011510149.2:c.30G>T
(GORAB)
|
XP_011508451.1:p.Ala10=
|
|
|
XM_011510150.3:c.-703G>T
(GORAB)
|
XP_011508452.1:n.-703G>T
|
|
|
XM_017002807.1:c.-764G>T
(GORAB)
|
XP_016858296.1:n.-764G>T
|
|
|
XM_024450864.1:c.-699G>T
(GORAB)
|
XP_024306632.1:n.-699G>T
|
|
|
NM_001146039.2:c.-46G>T
(GORAB)
|
NP_001139511.2:n.-46G>T
|
|
|
NM_001320252.2:c.-811G>T
(GORAB)
|
NP_001307181.1:n.-811G>T
|
|
|
NM_152281.3:c.-46G>T
(GORAB)
MANE Select
|
NP_689494.3:n.-46G>T
|
|
|
NR_027397.2:n.13G>T
(GORAB)
|
|
|
