|
ENST00000674112.2:c.2076G>T
(CUL7)
|
ENSP00000501166.2:p.Gln692His
|
|
|
ENST00000685042.1:c.2076G>T
(CUL7)
|
ENSP00000509871.1:p.Gln692His
|
|
|
ENST00000686442.1:n.2359G>T
(CUL7)
|
|
|
|
ENST00000687225.1:c.2172G>T
(CUL7)
|
ENSP00000509364.1:p.Gln724His
|
|
|
ENST00000688302.1:n.2359G>T
(CUL7)
|
|
|
|
ENST00000689256.1:n.2375G>T
(CUL7)
|
|
|
|
ENST00000690231.1:c.2076G>T
(CUL7)
|
ENSP00000508461.1:p.Gln692His
|
|
|
ENST00000265348.9:c.2076G>T
(CUL7)
MANE Select
|
ENSP00000265348.4:p.Gln692His
|
|
|
ENST00000673725.1:c.25G>T
(CUL7)
|
|
|
|
ENST00000673753.1:n.2410G>T
(CUL7)
|
|
|
|
ENST00000674100.1:c.2172G>T
(CUL7)
|
ENSP00000501292.1:p.Gln724His
|
|
|
ENST00000674112.1:c.568G>T
(CUL7)
|
|
|
|
ENST00000674134.1:c.2172G>T
(CUL7)
|
ENSP00000501068.1:p.Gln724His
|
|
|
ENST00000265348.7:c.2076G>T
(CUL7)
|
ENSP00000265348.3:p.Gln692His
|
|
|
ENST00000467906.5:c.-553+4733C>A
(KLC4)
|
ENSP00000418759.1:n.-553+4733C>A
|
|
|
ENST00000535468.1:c.2328G>T
(CUL7)
|
ENSP00000438788.1:p.Gln776His
|
|
|
NM_001168370.1:c.2328G>T
(CUL7)
|
NP_001161842.1:p.Gln776His
|
|
|
NM_014780.4:c.2076G>T
(CUL7)
|
NP_055595.2:p.Gln692His
|
|
|
XM_005249503.1:c.2232G>T
(CUL7)
|
XP_005249560.1:p.Gln744His
|
|
|
XM_006715285.1:c.2172G>T
(CUL7)
|
XP_006715348.1:p.Gln724His
|
|
|
XM_011515019.1:c.2328G>T
(CUL7)
|
XP_011513321.1:p.Gln776His
|
|
|
XM_011515020.1:c.2232G>T
(CUL7)
|
XP_011513322.1:p.Gln744His
|
|
|
XM_011515021.1:c.-107G>T
(CUL7)
|
XP_011513323.1:n.-107G>T
|
|
|
XM_005249503.3:c.2232G>T
(CUL7)
|
XP_005249560.1:p.Gln744His
|
|
|
XM_006715285.2:c.2172G>T
(CUL7)
|
XP_006715348.1:p.Gln724His
|
|
|
XM_011515019.2:c.2328G>T
(CUL7)
|
XP_011513321.1:p.Gln776His
|
|
|
XM_011515020.2:c.2232G>T
(CUL7)
|
XP_011513322.1:p.Gln744His
|
|
|
XM_017011533.1:c.2355G>T
(CUL7)
|
XP_016867022.1:p.Gln785His
|
|
|
XM_017011534.1:c.2355G>T
(CUL7)
|
XP_016867023.1:p.Gln785His
|
|
|
XM_017011535.1:c.2259G>T
(CUL7)
|
XP_016867024.1:p.Gln753His
|
|
|
XM_017011536.2:c.2199G>T
(CUL7)
|
XP_016867025.1:p.Gln733His
|
|
|
XM_017011537.2:c.2172G>T
(CUL7)
|
XP_016867026.1:p.Gln724His
|
|
|
XM_017011538.2:c.2103G>T
(CUL7)
|
XP_016867027.1:p.Gln701His
|
|
|
XM_017011539.2:c.2076G>T
(CUL7)
|
XP_016867028.1:p.Gln692His
|
|
|
XM_017011540.1:c.2355G>T
(CUL7)
|
XP_016867029.1:p.Gln785His
|
|
|
NM_001168370.2:c.2172G>T
(CUL7)
|
NP_001161842.2:p.Gln724His
|
|
|
NM_001374872.1:c.2172G>T
(CUL7)
|
NP_001361801.1:p.Gln724His
|
|
|
NM_001374873.1:c.2076G>T
(CUL7)
|
NP_001361802.1:p.Gln692His
|
|
|
NM_001374874.1:c.2076G>T
(CUL7)
|
NP_001361803.1:p.Gln692His
|
|
|
NM_014780.5:c.2076G>T
(CUL7)
MANE Select
|
NP_055595.2:p.Gln692His
|
|
