ENST00000621218.5:c.49G>T
(PLP1)
MANE Select
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ENSP00000484450.1:p.Ala17Ser
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ENST00000422393.5:c.49G>T
(PLP1)
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ENSP00000413931.1:p.Ala17Ser
|
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ENST00000433491.5:c.49G>T
(PLP1)
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ENSP00000393391.1:p.Ala17Ser
|
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ENST00000434483.5:c.49G>T
(PLP1)
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ENSP00000403335.1:p.Ala17Ser
|
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ENST00000443502.5:c.49G>T
(PLP1)
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ENSP00000391853.1:p.Ala17Ser
|
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ENST00000455268.5:c.49G>T
(PLP1)
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ENSP00000409802.1:p.Ala17Ser
|
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ENST00000464776.5:n.313G>T
(PLP1)
|
|
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ENST00000465975.1:n.171G>T
(PLP1)
|
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ENST00000479569.5:n.200G>T
(PLP1)
|
|
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ENST00000480325.1:n.128G>T
(PLP1)
|
|
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ENST00000485931.5:n.127G>T
(PLP1)
|
|
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ENST00000494475.5:c.49G>T
(PLP1)
|
ENSP00000480409.1:p.Ala17Ser
|
|
ENST00000495678.5:n.351G>T
(PLP1)
|
|
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ENST00000612423.4:c.49G>T
(PLP1)
|
ENSP00000481006.1:p.Ala17Ser
|
|
ENST00000619236.1:c.49G>T
(PLP1)
|
ENSP00000477619.1:p.Ala17Ser
|
|
ENST00000619257.4:n.279G>T
(PLP1)
|
|
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ENST00000621218.4:c.49G>T
(PLP1)
|
ENSP00000484450.1:p.Ala17Ser
|
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NM_000533.4:c.49G>T
(PLP1)
|
NP_000524.3:p.Ala17Ser
|
|
NM_001128834.2:c.49G>T
(PLP1)
|
NP_001122306.1:p.Ala17Ser
|
|
NM_001305004.1:c.5-121G>T
(PLP1)
|
NP_001291933.1:n.5-121G>T
|
|
NM_199478.2:c.49G>T
(PLP1)
|
NP_955772.1:p.Ala17Ser
|
|
XR_244483.3:n.862+7055C>A
|
|
|
NR_146558.1:n.457+7055C>A
(RAB9B)
|
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NR_146560.1:n.743+7055C>A
(RAB9B)
|
|
|
NM_000533.5:c.49G>T
(PLP1)
MANE Select
|
NP_000524.3:p.Ala17Ser
|
|
NM_199478.3:c.49G>T
(PLP1)
|
NP_955772.1:p.Ala17Ser
|
|
NM_001128834.3:c.49G>T
(PLP1)
|
NP_001122306.1:p.Ala17Ser
|
|
NR_146558.2:n.432+7055C>A
(RAB9B)
|
|
|
NR_146560.2:n.718+7055C>A
(RAB9B)
|
|
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