ENST00000383820.10:c.704T>C
(RPUSD3)
MANE Select
|
ENSP00000373331.6:p.Phe235Ser
|
|
ENST00000433535.7:c.659T>C
(RPUSD3)
|
ENSP00000398921.3:p.Phe220Ser
|
|
ENST00000383820.9:c.728T>C
(RPUSD3)
|
ENSP00000373331.5:p.Phe243Ser
|
|
ENST00000423108.5:c.214T>C
(RPUSD3)
|
|
|
ENST00000424438.5:c.629-961T>C
(RPUSD3)
|
ENSP00000408693.1:n.629-961T>C
|
|
ENST00000427174.5:c.728T>C
(RPUSD3)
|
|
|
ENST00000433535.6:c.683T>C
(RPUSD3)
|
ENSP00000398921.2:p.Phe228Ser
|
|
ENST00000455274.5:c.918+9773A>G
(TTLL3)
|
ENSP00000409632.1:n.918+9773A>G
|
|
ENST00000464783.1:n.687T>C
(RPUSD3)
|
|
|
ENST00000466141.1:n.546T>C
(RPUSD3)
|
|
|
NM_001142547.1:c.683T>C
(RPUSD3)
|
NP_001136019.1:p.Phe228Ser
|
|
NM_173659.3:c.728T>C
(RPUSD3)
|
NP_775930.2:p.Phe243Ser
|
|
XM_011533627.1:c.725-961T>C
(RPUSD3)
|
XP_011531929.1:n.725-961T>C
|
|
NM_001142547.2:c.683T>C
(RPUSD3)
|
NP_001136019.1:p.Phe228Ser
|
|
NM_001351736.1:c.629-961T>C
(RPUSD3)
|
NP_001338665.1:n.629-961T>C
|
|
NM_001351737.1:c.725-961T>C
(RPUSD3)
|
NP_001338666.1:n.725-961T>C
|
|
NM_001351738.1:c.756T>C
(RPUSD3)
|
NP_001338667.1:p.Val252=
|
|
NM_173659.4:c.728T>C
(RPUSD3)
|
NP_775930.2:p.Phe243Ser
|
|
XM_024453471.1:c.728T>C
(RPUSD3)
|
XP_024309239.1:p.Phe243Ser
|
|
XM_024453472.1:c.724+1016T>C
(RPUSD3)
|
XP_024309240.1:n.724+1016T>C
|
|
NM_001351736.2:c.629-961T>C
(RPUSD3)
|
NP_001338665.1:n.629-961T>C
|
|
NM_001351736.3:c.629-961T>C
(RPUSD3)
|
NP_001338665.1:n.629-961T>C
|
|
NM_001142547.3:c.659T>C
(RPUSD3)
|
NP_001136019.2:p.Phe220Ser
|
|
NM_001351737.2:c.701-961T>C
(RPUSD3)
|
NP_001338666.2:n.701-961T>C
|
|
NM_001351738.2:c.732T>C
(RPUSD3)
|
NP_001338667.2:p.Val244=
|
|
NM_173659.5:c.704T>C
(RPUSD3)
MANE Select
|
NP_775930.3:p.Phe235Ser
|
|