ENST00000682888.1:c.369T>G
(PHEX)
|
ENSP00000508003.1:p.Thr123=
|
|
ENST00000683162.1:c.369T>G
(PHEX)
|
ENSP00000508059.1:p.Thr123=
|
|
ENST00000683289.1:c.369T>G
(PHEX)
|
ENSP00000508195.1:p.Thr123=
|
|
ENST00000683917.1:n.599T>G
(PHEX)
|
|
|
ENST00000684356.1:c.369T>G
(PHEX)
|
ENSP00000507619.1:p.Thr123=
|
|
ENST00000684745.1:n.1489T>G
(PHEX)
|
|
|
ENST00000379374.5:c.1815T>G
(PHEX)
MANE Select
|
ENSP00000368682.4:p.Thr605=
|
|
ENST00000379374.4:c.1815T>G
(PHEX)
|
ENSP00000368682.4:p.Thr605=
|
|
NM_000444.5:c.1815T>G
(PHEX)
|
NP_000435.3:p.Thr605=
|
|
NM_001282754.1:c.1815T>G
(PHEX)
|
NP_001269683.1:p.Thr605=
|
|
XM_011545533.1:c.1059T>G
(PHEX)
|
XP_011543835.1:p.Thr353=
|
|
XM_011545534.1:c.1059T>G
(PHEX)
|
XP_011543836.1:p.Thr353=
|
|
XM_011545536.1:c.708T>G
(PHEX)
|
XP_011543838.1:p.Thr236=
|
|
NR_073010.2:n.1048+5811A>C
(PTCHD1-AS)
|
|
|
XM_011545536.2:c.708T>G
(PHEX)
|
XP_011543838.1:p.Thr236=
|
|
XM_017029579.1:c.1059T>G
(PHEX)
|
XP_016885068.1:p.Thr353=
|
|
XM_024452390.1:c.1524T>G
(PHEX)
|
XP_024308158.1:p.Thr508=
|
|
XR_001755695.1:n.2655T>G
(PHEX)
|
|
|
NM_000444.6:c.1815T>G
(PHEX)
MANE Select
|
NP_000435.3:p.Thr605=
|
|
NM_001282754.2:c.1815T>G
(PHEX)
|
NP_001269683.1:p.Thr605=
|
|