ENST00000683162.1:c.*370T>C
(PHEX)
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ENSP00000508059.1:n.*370T>C
|
|
ENST00000683289.1:c.624+20524T>C
(PHEX)
|
ENSP00000508195.1:n.624+20524T>C
|
|
ENST00000683917.1:n.1158+58T>C
(PHEX)
|
|
|
ENST00000684356.1:c.*182T>C
(PHEX)
|
ENSP00000507619.1:n.*182T>C
|
|
ENST00000684745.1:n.2106T>C
(PHEX)
|
|
|
ENST00000379374.5:c.*182T>C
(PHEX)
MANE Select
|
ENSP00000368682.4:n.*182T>C
|
|
ENST00000379374.4:c.*182T>C
(PHEX)
|
ENSP00000368682.4:n.*182T>C
|
|
NM_000444.5:c.*182T>C
(PHEX)
|
NP_000435.3:n.*182T>C
|
|
NM_001282754.1:c.*267T>C
(PHEX)
|
NP_001269683.1:n.*267T>C
|
|
XM_011545533.1:c.*182T>C
(PHEX)
|
XP_011543835.1:n.*182T>C
|
|
XM_011545534.1:c.*182T>C
(PHEX)
|
XP_011543836.1:n.*182T>C
|
|
XM_011545536.1:c.*182T>C
(PHEX)
|
XP_011543838.1:n.*182T>C
|
|
XR_950533.1:n.140+5804A>G
|
|
|
XR_950534.1:n.127+5804A>G
|
|
|
NR_073010.2:n.850+5804A>G
(PTCHD1-AS)
|
|
|
XM_011545536.2:c.*182T>C
(PHEX)
|
XP_011543838.1:n.*182T>C
|
|
XM_017029579.1:c.*182T>C
(PHEX)
|
XP_016885068.1:n.*182T>C
|
|
XM_024452390.1:c.*182T>C
(PHEX)
|
XP_024308158.1:n.*182T>C
|
|
XR_001755695.1:n.3272T>C
(PHEX)
|
|
|
NM_000444.6:c.*182T>C
(PHEX)
MANE Select
|
NP_000435.3:n.*182T>C
|
|
NM_001282754.2:c.*267T>C
(PHEX)
|
NP_001269683.1:n.*267T>C
|
|