|
ENST00000621218.5:c.418C>T
(PLP1)
MANE Select
|
ENSP00000484450.1:p.His140Tyr
|
|
|
ENST00000461231.5:n.264+70C>T
(PLP1)
|
|
|
|
ENST00000465975.1:n.312-36C>T
(PLP1)
|
|
|
|
ENST00000476160.1:n.397C>T
(PLP1)
|
|
|
|
ENST00000478642.5:n.399C>T
(PLP1)
|
|
|
|
ENST00000479569.5:n.499+70C>T
(PLP1)
|
|
|
|
ENST00000485688.5:n.190+70C>T
(PLP1)
|
|
|
|
ENST00000485931.5:n.496C>T
(PLP1)
|
|
|
|
ENST00000612423.4:c.418C>T
(PLP1)
|
ENSP00000481006.1:p.His140Tyr
|
|
|
ENST00000619236.1:c.348+70C>T
(PLP1)
|
ENSP00000477619.1:n.348+70C>T
|
|
|
ENST00000621218.4:c.418C>T
(PLP1)
|
ENSP00000484450.1:p.His140Tyr
|
|
|
NM_000533.4:c.418C>T
(PLP1)
|
NP_000524.3:p.His140Tyr
|
|
|
NM_001128834.2:c.418C>T
(PLP1)
|
NP_001122306.1:p.His140Tyr
|
|
|
NM_001305004.1:c.253C>T
(PLP1)
|
NP_001291933.1:p.His85Tyr
|
|
|
NM_199478.2:c.348+70C>T
(PLP1)
|
NP_955772.1:n.348+70C>T
|
|
|
XR_244483.3:n.862+5990G>A
|
|
|
|
NR_146558.1:n.457+5990G>A
(RAB9B)
|
|
|
|
NR_146560.1:n.743+5990G>A
(RAB9B)
|
|
|
|
NM_000533.5:c.418C>T
(PLP1)
MANE Select
|
NP_000524.3:p.His140Tyr
|
|
|
NM_199478.3:c.348+70C>T
(PLP1)
|
NP_955772.1:n.348+70C>T
|
|
|
NM_001128834.3:c.418C>T
(PLP1)
|
NP_001122306.1:p.His140Tyr
|
|
|
NR_146558.2:n.432+5990G>A
(RAB9B)
|
|
|
|
NR_146560.2:n.718+5990G>A
(RAB9B)
|
|
|
