ENST00000682888.1:c.489T=
(PHEX)
|
ENSP00000508003.1:p.Ala163=
|
|
ENST00000683162.1:c.489T=
(PHEX)
|
ENSP00000508059.1:p.Ala163=
|
|
ENST00000683289.1:c.489T=
(PHEX)
|
ENSP00000508195.1:p.Ala163=
|
|
ENST00000683917.1:n.719T=
(PHEX)
|
|
|
ENST00000684356.1:c.489T=
(PHEX)
|
ENSP00000507619.1:p.Ala163=
|
|
ENST00000684745.1:n.1609T=
(PHEX)
|
|
|
ENST00000379374.5:c.1935T=
(PHEX)
MANE Select
|
ENSP00000368682.4:p.Ala645=
|
|
ENST00000379374.4:c.1935T=
(PHEX)
|
ENSP00000368682.4:p.Ala645=
|
|
NM_000444.5:c.1935T=
(PHEX)
|
NP_000435.3:p.Ala645=
|
|
NM_001282754.1:c.1935T=
(PHEX)
|
NP_001269683.1:p.Ala645=
|
|
XM_011545533.1:c.1179T=
(PHEX)
|
XP_011543835.1:p.Ala393=
|
|
XM_011545534.1:c.1179T=
(PHEX)
|
XP_011543836.1:p.Ala393=
|
|
XM_011545536.1:c.828T=
(PHEX)
|
XP_011543838.1:p.Ala276=
|
|
XR_950534.1:n.326-455A=
|
|
|
NR_073010.2:n.1048+992A=
(PTCHD1-AS)
|
|
|
XM_011545536.2:c.828T=
(PHEX)
|
XP_011543838.1:p.Ala276=
|
|
XM_017029579.1:c.1179T=
(PHEX)
|
XP_016885068.1:p.Ala393=
|
|
XM_024452390.1:c.1644T=
(PHEX)
|
XP_024308158.1:p.Ala548=
|
|
XR_001755695.1:n.2775T=
(PHEX)
|
|
|
NM_000444.6:c.1935T=
(PHEX)
MANE Select
|
NP_000435.3:p.Ala645=
|
|
NM_001282754.2:c.1935T=
(PHEX)
|
NP_001269683.1:p.Ala645=
|
|