ENST00000683162.1:c.*474T>C
(PHEX)
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ENSP00000508059.1:n.*474T>C
|
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ENST00000683289.1:c.624+20628T>C
(PHEX)
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ENSP00000508195.1:n.624+20628T>C
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ENST00000683917.1:n.1158+162T>C
(PHEX)
|
|
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ENST00000684356.1:c.*286T>C
(PHEX)
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ENSP00000507619.1:n.*286T>C
|
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ENST00000684745.1:n.2210T>C
(PHEX)
|
|
|
ENST00000379374.5:c.*286T>C
(PHEX)
MANE Select
|
ENSP00000368682.4:n.*286T>C
|
|
ENST00000379374.4:c.*286T>C
(PHEX)
|
ENSP00000368682.4:n.*286T>C
|
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NM_000444.5:c.*286T>C
(PHEX)
|
NP_000435.3:n.*286T>C
|
|
NM_001282754.1:c.*371T>C
(PHEX)
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NP_001269683.1:n.*371T>C
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XM_011545533.1:c.*286T>C
(PHEX)
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XP_011543835.1:n.*286T>C
|
|
XM_011545534.1:c.*286T>C
(PHEX)
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XP_011543836.1:n.*286T>C
|
|
XM_011545536.1:c.*286T>C
(PHEX)
|
XP_011543838.1:n.*286T>C
|
|
XR_950533.1:n.140+5700A>G
|
|
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XR_950534.1:n.127+5700A>G
|
|
|
NR_073010.2:n.850+5700A>G
(PTCHD1-AS)
|
|
|
XM_011545536.2:c.*286T>C
(PHEX)
|
XP_011543838.1:n.*286T>C
|
|
XM_017029579.1:c.*286T>C
(PHEX)
|
XP_016885068.1:n.*286T>C
|
|
XM_024452390.1:c.*286T>C
(PHEX)
|
XP_024308158.1:n.*286T>C
|
|
XR_001755695.1:n.3376T>C
(PHEX)
|
|
|
NM_000444.6:c.*286T>C
(PHEX)
MANE Select
|
NP_000435.3:n.*286T>C
|
|
NM_001282754.2:c.*371T>C
(PHEX)
|
NP_001269683.1:n.*371T>C
|
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