ENST00000683162.1:c.*98A>T
(PHEX)
|
ENSP00000508059.1:n.*98A>T
|
|
ENST00000683289.1:c.624+20252A>T
(PHEX)
|
ENSP00000508195.1:n.624+20252A>T
|
|
ENST00000683917.1:n.944A>T
(PHEX)
|
|
|
ENST00000684356.1:c.714A>T
(PHEX)
|
ENSP00000507619.1:p.Ala238=
|
|
ENST00000684745.1:n.1834A>T
(PHEX)
|
|
|
ENST00000379374.5:c.2160A>T
(PHEX)
MANE Select
|
ENSP00000368682.4:p.Ala720=
|
|
ENST00000379374.4:c.2160A>T
(PHEX)
|
ENSP00000368682.4:p.Ala720=
|
|
NM_000444.5:c.2160A>T
(PHEX)
|
NP_000435.3:p.Ala720=
|
|
NM_001282754.1:c.2083A>T
(PHEX)
|
NP_001269683.1:p.Asn695Tyr
|
|
XM_011545533.1:c.1404A>T
(PHEX)
|
XP_011543835.1:p.Ala468=
|
|
XM_011545534.1:c.1404A>T
(PHEX)
|
XP_011543836.1:p.Ala468=
|
|
XM_011545536.1:c.1053A>T
(PHEX)
|
XP_011543838.1:p.Ala351=
|
|
XR_950533.1:n.140+6076T>A
|
|
|
XR_950534.1:n.127+6076T>A
|
|
|
NR_073010.2:n.850+6076T>A
(PTCHD1-AS)
|
|
|
XM_011545536.2:c.1053A>T
(PHEX)
|
XP_011543838.1:p.Ala351=
|
|
XM_017029579.1:c.1404A>T
(PHEX)
|
XP_016885068.1:p.Ala468=
|
|
XM_024452390.1:c.1869A>T
(PHEX)
|
XP_024308158.1:p.Ala623=
|
|
XR_001755695.1:n.3000A>T
(PHEX)
|
|
|
NM_000444.6:c.2160A>T
(PHEX)
MANE Select
|
NP_000435.3:p.Ala720=
|
|
NM_001282754.2:c.2083A>T
(PHEX)
|
NP_001269683.1:p.Asn695Tyr
|
|