ENST00000683162.1:c.*97C>A
(PHEX)
|
ENSP00000508059.1:n.*97C>A
|
|
ENST00000683289.1:c.624+20251C>A
(PHEX)
|
ENSP00000508195.1:n.624+20251C>A
|
|
ENST00000683917.1:n.943C>A
(PHEX)
|
|
|
ENST00000684356.1:c.713C>A
(PHEX)
|
ENSP00000507619.1:p.Ala238Glu
|
|
ENST00000684745.1:n.1833C>A
(PHEX)
|
|
|
ENST00000379374.5:c.2159C>A
(PHEX)
MANE Select
|
ENSP00000368682.4:p.Ala720Glu
|
|
ENST00000379374.4:c.2159C>A
(PHEX)
|
ENSP00000368682.4:p.Ala720Glu
|
|
NM_000444.5:c.2159C>A
(PHEX)
|
NP_000435.3:p.Ala720Glu
|
|
NM_001282754.1:c.2082C>A
(PHEX)
|
NP_001269683.1:p.Cys694Ter
|
|
XM_011545533.1:c.1403C>A
(PHEX)
|
XP_011543835.1:p.Ala468Glu
|
|
XM_011545534.1:c.1403C>A
(PHEX)
|
XP_011543836.1:p.Ala468Glu
|
|
XM_011545536.1:c.1052C>A
(PHEX)
|
XP_011543838.1:p.Ala351Glu
|
|
XR_950533.1:n.140+6077G>T
|
|
|
XR_950534.1:n.127+6077G>T
|
|
|
NR_073010.2:n.850+6077G>T
(PTCHD1-AS)
|
|
|
XM_011545536.2:c.1052C>A
(PHEX)
|
XP_011543838.1:p.Ala351Glu
|
|
XM_017029579.1:c.1403C>A
(PHEX)
|
XP_016885068.1:p.Ala468Glu
|
|
XM_024452390.1:c.1868C>A
(PHEX)
|
XP_024308158.1:p.Ala623Glu
|
|
XR_001755695.1:n.2999C>A
(PHEX)
|
|
|
NM_000444.6:c.2159C>A
(PHEX)
MANE Select
|
NP_000435.3:p.Ala720Glu
|
|
NM_001282754.2:c.2082C>A
(PHEX)
|
NP_001269683.1:p.Cys694Ter
|
|