|
ENST00000621218.5:c.205C>T
(PLP1)
MANE Select
|
ENSP00000484450.1:p.Gln69Ter
|
|
|
ENST00000422393.5:c.205C>T
(PLP1)
|
ENSP00000413931.1:p.Gln69Ter
|
|
|
ENST00000433491.5:c.205C>T
(PLP1)
|
ENSP00000393391.1:p.Gln69Ter
|
|
|
ENST00000434483.5:c.205C>T
(PLP1)
|
ENSP00000403335.1:p.Gln69Ter
|
|
|
ENST00000443502.5:c.205C>T
(PLP1)
|
ENSP00000391853.1:p.Gln69Ter
|
|
|
ENST00000455268.5:c.205C>T
(PLP1)
|
ENSP00000409802.1:p.Gln69Ter
|
|
|
ENST00000461231.5:n.121C>T
(PLP1)
|
|
|
|
ENST00000464776.5:n.469C>T
(PLP1)
|
|
|
|
ENST00000465975.1:n.312-249C>T
(PLP1)
|
|
|
|
ENST00000476160.1:n.184C>T
(PLP1)
|
|
|
|
ENST00000478642.5:n.186C>T
(PLP1)
|
|
|
|
ENST00000479569.5:n.356C>T
(PLP1)
|
|
|
|
ENST00000485688.5:n.47C>T
(PLP1)
|
|
|
|
ENST00000485931.5:n.283C>T
(PLP1)
|
|
|
|
ENST00000494475.5:c.205C>T
(PLP1)
|
ENSP00000480409.1:p.Gln69Ter
|
|
|
ENST00000495678.5:n.507C>T
(PLP1)
|
|
|
|
ENST00000612423.4:c.205C>T
(PLP1)
|
ENSP00000481006.1:p.Gln69Ter
|
|
|
ENST00000619236.1:c.205C>T
(PLP1)
|
ENSP00000477619.1:p.Gln69Ter
|
|
|
ENST00000619257.4:n.435C>T
(PLP1)
|
|
|
|
ENST00000621218.4:c.205C>T
(PLP1)
|
ENSP00000484450.1:p.Gln69Ter
|
|
|
NM_000533.4:c.205C>T
(PLP1)
|
NP_000524.3:p.Gln69Ter
|
|
|
NM_001128834.2:c.205C>T
(PLP1)
|
NP_001122306.1:p.Gln69Ter
|
|
|
NM_001305004.1:c.40C>T
(PLP1)
|
NP_001291933.1:p.Gln14Ter
|
|
|
NM_199478.2:c.205C>T
(PLP1)
|
NP_955772.1:p.Gln69Ter
|
|
|
XR_244483.3:n.862+6203G>A
|
|
|
|
NR_146558.1:n.457+6203G>A
(RAB9B)
|
|
|
|
NR_146560.1:n.743+6203G>A
(RAB9B)
|
|
|
|
NM_000533.5:c.205C>T
(PLP1)
MANE Select
|
NP_000524.3:p.Gln69Ter
|
|
|
NM_199478.3:c.205C>T
(PLP1)
|
NP_955772.1:p.Gln69Ter
|
|
|
NM_001128834.3:c.205C>T
(PLP1)
|
NP_001122306.1:p.Gln69Ter
|
|
|
NR_146558.2:n.432+6203G>A
(RAB9B)
|
|
|
|
NR_146560.2:n.718+6203G>A
(RAB9B)
|
|
|
