ENST00000682888.1:c.295G>T
(PHEX)
|
ENSP00000508003.1:p.Glu99Ter
|
|
ENST00000683162.1:c.295G>T
(PHEX)
|
ENSP00000508059.1:p.Glu99Ter
|
|
ENST00000683289.1:c.295G>T
(PHEX)
|
ENSP00000508195.1:p.Glu99Ter
|
|
ENST00000683917.1:n.525G>T
(PHEX)
|
|
|
ENST00000684356.1:c.295G>T
(PHEX)
|
ENSP00000507619.1:p.Glu99Ter
|
|
ENST00000684745.1:n.1415G>T
(PHEX)
|
|
|
ENST00000379374.5:c.1741G>T
(PHEX)
MANE Select
|
ENSP00000368682.4:p.Glu581Ter
|
|
ENST00000379374.4:c.1741G>T
(PHEX)
|
ENSP00000368682.4:p.Glu581Ter
|
|
NM_000444.5:c.1741G>T
(PHEX)
|
NP_000435.3:p.Glu581Ter
|
|
NM_001282754.1:c.1741G>T
(PHEX)
|
NP_001269683.1:p.Glu581Ter
|
|
XM_011545533.1:c.985G>T
(PHEX)
|
XP_011543835.1:p.Glu329Ter
|
|
XM_011545534.1:c.985G>T
(PHEX)
|
XP_011543836.1:p.Glu329Ter
|
|
XM_011545536.1:c.634G>T
(PHEX)
|
XP_011543838.1:p.Glu212Ter
|
|
NR_073010.2:n.1048+8394C>A
(PTCHD1-AS)
|
|
|
XM_011545536.2:c.634G>T
(PHEX)
|
XP_011543838.1:p.Glu212Ter
|
|
XM_017029579.1:c.985G>T
(PHEX)
|
XP_016885068.1:p.Glu329Ter
|
|
XM_024452390.1:c.1450G>T
(PHEX)
|
XP_024308158.1:p.Glu484Ter
|
|
XR_001755695.1:n.2581G>T
(PHEX)
|
|
|
NM_000444.6:c.1741G>T
(PHEX)
MANE Select
|
NP_000435.3:p.Glu581Ter
|
|
NM_001282754.2:c.1741G>T
(PHEX)
|
NP_001269683.1:p.Glu581Ter
|
|