|
ENST00000226105.11:c.139C>T
(RANGRF)
MANE Select
|
ENSP00000226105.6:p.Leu47=
|
|
|
ENST00000226105.10:c.139C>T
(RANGRF)
|
ENSP00000226105.6:p.Leu47=
|
|
|
ENST00000380067.6:c.*599G>A
(SLC25A35)
|
ENSP00000369407.2:n.*599G>A
|
|
|
ENST00000407006.8:c.139C>T
(RANGRF)
|
ENSP00000383940.4:p.Leu47=
|
|
|
ENST00000439238.3:c.139C>T
(RANGRF)
|
ENSP00000413190.3:p.Leu47=
|
|
|
ENST00000578849.1:n.229C>T
(RANGRF)
|
|
|
|
ENST00000579192.5:c.*42+557G>A
(SLC25A35)
|
ENSP00000462395.1:n.*42+557G>A
|
|
|
ENST00000580340.5:c.*466G>A
(SLC25A35)
|
ENSP00000464071.1:n.*466G>A
|
|
|
ENST00000580434.5:c.139C>T
(RANGRF)
|
ENSP00000462310.1:p.Leu47=
|
|
|
ENST00000580777.1:n.133C>T
(RANGRF)
|
|
|
|
ENST00000581320.1:n.19G>A
(SLC25A35)
|
|
|
|
ENST00000585311.5:c.*511G>A
(SLC25A35)
|
ENSP00000464191.1:n.*511G>A
|
|
|
NM_001177801.1:c.139C>T
(RANGRF)
|
NP_001171272.1:p.Leu47=
|
|
|
NM_001177802.1:c.139C>T
(RANGRF)
|
NP_001171273.1:p.Leu47=
|
|
|
NM_016492.4:c.139C>T
(RANGRF)
|
NP_057576.2:p.Leu47=
|
|
|
NM_201520.1:c.*599G>A
(SLC25A35)
|
NP_958928.1:n.*599G>A
|
|
|
XM_005256618.3:c.139C>T
(RANGRF)
|
XP_005256675.1:p.Leu47=
|
|
|
NM_001320871.1:c.*42+557G>A
(SLC25A35)
|
NP_001307800.1:n.*42+557G>A
|
|
|
NM_001320872.1:c.*466G>A
(SLC25A35)
|
NP_001307801.1:n.*466G>A
|
|
|
NM_001330127.1:c.139C>T
(RANGRF)
|
NP_001317056.1:p.Leu47=
|
|
|
NM_201520.2:c.*599G>A
(SLC25A35)
|
NP_958928.1:n.*599G>A
|
|
|
NR_135484.1:n.1923G>A
(SLC25A35)
|
|
|
|
NM_016492.5:c.139C>T
(RANGRF)
MANE Select
|
NP_057576.2:p.Leu47=
|
|
|
NM_001177801.2:c.139C>T
(RANGRF)
|
NP_001171272.1:p.Leu47=
|
|
|
NM_001177802.2:c.139C>T
(RANGRF)
|
NP_001171273.1:p.Leu47=
|
|
|
NM_001320871.2:c.*42+557G>A
(SLC25A35)
|
NP_001307800.1:n.*42+557G>A
|
|
|
NM_001330127.2:c.139C>T
(RANGRF)
|
NP_001317056.1:p.Leu47=
|
|
|
NM_201520.3:c.*599G>A
(SLC25A35)
|
NP_958928.1:n.*599G>A
|
|
|
NR_135483.2:n.2144G>A
(SLC25A35)
|
|
|
|
NM_001320872.2:c.*466G>A
(SLC25A35)
|
NP_001307801.1:n.*466G>A
|
|
|
NR_135484.2:n.1980G>A
(SLC25A35)
|
|
|
