ENST00000683162.1:c.*468T>C
(PHEX)
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ENSP00000508059.1:n.*468T>C
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ENST00000683289.1:c.624+20622T>C
(PHEX)
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ENSP00000508195.1:n.624+20622T>C
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ENST00000683917.1:n.1158+156T>C
(PHEX)
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ENST00000684356.1:c.*280T>C
(PHEX)
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ENSP00000507619.1:n.*280T>C
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ENST00000684745.1:n.2204T>C
(PHEX)
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ENST00000379374.5:c.*280T>C
(PHEX)
MANE Select
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ENSP00000368682.4:n.*280T>C
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ENST00000379374.4:c.*280T>C
(PHEX)
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ENSP00000368682.4:n.*280T>C
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NM_000444.5:c.*280T>C
(PHEX)
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NP_000435.3:n.*280T>C
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NM_001282754.1:c.*365T>C
(PHEX)
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NP_001269683.1:n.*365T>C
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XM_011545533.1:c.*280T>C
(PHEX)
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XP_011543835.1:n.*280T>C
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XM_011545534.1:c.*280T>C
(PHEX)
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XP_011543836.1:n.*280T>C
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XM_011545536.1:c.*280T>C
(PHEX)
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XP_011543838.1:n.*280T>C
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XR_950533.1:n.140+5706A>G
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XR_950534.1:n.127+5706A>G
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NR_073010.2:n.850+5706A>G
(PTCHD1-AS)
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XM_011545536.2:c.*280T>C
(PHEX)
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XP_011543838.1:n.*280T>C
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XM_017029579.1:c.*280T>C
(PHEX)
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XP_016885068.1:n.*280T>C
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XM_024452390.1:c.*280T>C
(PHEX)
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XP_024308158.1:n.*280T>C
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XR_001755695.1:n.3370T>C
(PHEX)
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|
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NM_000444.6:c.*280T>C
(PHEX)
MANE Select
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NP_000435.3:n.*280T>C
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NM_001282754.2:c.*365T>C
(PHEX)
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NP_001269683.1:n.*365T>C
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