|
ENST00000397098.8:c.130-47495G>A
(C7orf50)
MANE Select
|
ENSP00000380286.3:n.130-47495G>A
|
|
|
ENST00000444847.2:c.123C>T
(GPR146)
MANE Select
|
ENSP00000410743.2:p.Gly41=
|
|
|
ENST00000297468.3:c.123C>T
(GPR146)
|
ENSP00000297468.3:p.Gly41=
|
|
|
ENST00000357429.10:c.130-47495G>A
(C7orf50)
|
ENSP00000350011.5:n.130-47495G>A
|
|
|
ENST00000397095.2:c.123C>T
(GPR146)
|
ENSP00000380283.1:p.Gly41=
|
|
|
ENST00000397098.7:c.130-47495G>A
(C7orf50)
|
ENSP00000380286.3:n.130-47495G>A
|
|
|
ENST00000397100.6:c.130-47495G>A
(C7orf50)
|
ENSP00000380288.2:n.130-47495G>A
|
|
|
ENST00000444847.1:c.123C>T
(GPR146)
|
ENSP00000410743.1:p.Gly41=
|
|
|
ENST00000488073.1:n.267-47495G>A
(C7orf50)
|
|
|
|
ENST00000491163.1:c.130-47495G>A
(C7orf50)
|
ENSP00000420130.1:n.130-47495G>A
|
|
|
NM_001134395.1:c.130-47495G>A
(C7orf50)
|
NP_001127867.1:n.130-47495G>A
|
|
|
NM_001134396.1:c.130-47495G>A
(C7orf50)
|
NP_001127868.1:n.130-47495G>A
|
|
|
NM_001303473.1:c.123C>T
(GPR146)
|
NP_001290402.1:p.Gly41=
|
|
|
NM_001303474.1:c.123C>T
(GPR146)
|
NP_001290403.1:p.Gly41=
|
|
|
NM_032350.5:c.130-47495G>A
(C7orf50)
|
NP_115726.1:n.130-47495G>A
|
|
|
NM_138445.3:c.123C>T
(GPR146)
|
NP_612454.1:p.Gly41=
|
|
|
XM_005249613.1:c.759C>T
(GPR146)
|
XP_005249670.1:p.Gly253=
|
|
|
XM_005249888.3:c.130-47495G>A
(C7orf50)
|
XP_005249945.1:n.130-47495G>A
|
|
|
XM_006715642.1:c.177C>T
(GPR146)
|
XP_006715705.1:p.Gly59=
|
|
|
XM_006715643.1:c.123C>T
(GPR146)
|
XP_006715706.1:p.Gly41=
|
|
|
XM_011515116.1:c.177C>T
(GPR146)
|
XP_011513418.1:p.Gly59=
|
|
|
XM_011515581.1:c.130-47495G>A
(C7orf50)
|
XP_011513883.1:n.130-47495G>A
|
|
|
XM_011515582.1:c.130-47495G>A
(C7orf50)
|
XP_011513884.1:n.130-47495G>A
|
|
|
XM_011515583.1:c.130-47495G>A
(C7orf50)
|
XP_011513885.1:n.130-47495G>A
|
|
|
XM_011515584.1:c.130-47495G>A
(C7orf50)
|
XP_011513886.1:n.130-47495G>A
|
|
|
NM_001318252.1:c.130-47495G>A
(C7orf50)
|
NP_001305181.1:n.130-47495G>A
|
|
|
NM_001350968.1:c.130-47495G>A
(C7orf50)
|
NP_001337897.1:n.130-47495G>A
|
|
|
XM_005249613.3:c.123C>T
(GPR146)
|
XP_005249670.2:p.Gly41=
|
|
|
XM_006715642.2:c.177C>T
(GPR146)
|
XP_006715705.1:p.Gly59=
|
|
|
XM_006715643.2:c.123C>T
(GPR146)
|
XP_006715706.1:p.Gly41=
|
|
|
XM_011515116.3:c.177C>T
(GPR146)
|
XP_011513418.1:p.Gly59=
|
|
|
XM_011515581.3:c.130-47495G>A
(C7orf50)
|
XP_011513883.1:n.130-47495G>A
|
|
|
XM_011515582.3:c.130-47495G>A
(C7orf50)
|
XP_011513884.1:n.130-47495G>A
|
|
|
XM_011515583.2:c.130-47495G>A
(C7orf50)
|
XP_011513885.1:n.130-47495G>A
|
|
|
XM_011515584.2:c.130-47495G>A
(C7orf50)
|
XP_011513886.1:n.130-47495G>A
|
|
|
XM_017012720.2:c.130-47495G>A
(C7orf50)
|
XP_016868209.1:n.130-47495G>A
|
|
|
XM_017012721.2:c.-144-36047G>A
(C7orf50)
|
XP_016868210.1:n.-144-36047G>A
|
|
|
XM_024446977.1:c.130-47495G>A
(C7orf50)
|
XP_024302745.1:n.130-47495G>A
|
|
|
XM_024446978.1:c.-144-36047G>A
(C7orf50)
|
XP_024302746.1:n.-144-36047G>A
|
|
|
NM_001303473.2:c.123C>T
(GPR146)
MANE Select
|
NP_001290402.1:p.Gly41=
|
|
|
NM_001318252.2:c.130-47495G>A
(C7orf50)
MANE Select
|
NP_001305181.1:n.130-47495G>A
|
|
|
NM_001303474.2:c.123C>T
(GPR146)
|
NP_001290403.1:p.Gly41=
|
|
|
NM_138445.4:c.123C>T
(GPR146)
|
NP_612454.1:p.Gly41=
|
|
