ENST00000383820.10:c.739C>G
(RPUSD3)
MANE Select
|
ENSP00000373331.6:p.Leu247Val
|
|
ENST00000433535.7:c.694C>G
(RPUSD3)
|
ENSP00000398921.3:p.Leu232Val
|
|
ENST00000383820.9:c.763C>G
(RPUSD3)
|
ENSP00000373331.5:p.Leu255Val
|
|
ENST00000423108.5:c.249C>G
(RPUSD3)
|
|
|
ENST00000424438.5:c.629-926C>G
(RPUSD3)
|
ENSP00000408693.1:n.629-926C>G
|
|
ENST00000427174.5:c.763C>G
(RPUSD3)
|
|
|
ENST00000433535.6:c.718C>G
(RPUSD3)
|
ENSP00000398921.2:p.Leu240Val
|
|
ENST00000455274.5:c.918+9738G>C
(TTLL3)
|
ENSP00000409632.1:n.918+9738G>C
|
|
ENST00000464783.1:n.722C>G
(RPUSD3)
|
|
|
ENST00000466141.1:n.581C>G
(RPUSD3)
|
|
|
NM_001142547.1:c.718C>G
(RPUSD3)
|
NP_001136019.1:p.Leu240Val
|
|
NM_173659.3:c.763C>G
(RPUSD3)
|
NP_775930.2:p.Leu255Val
|
|
XM_011533627.1:c.725-926C>G
(RPUSD3)
|
XP_011531929.1:n.725-926C>G
|
|
NM_001142547.2:c.718C>G
(RPUSD3)
|
NP_001136019.1:p.Leu240Val
|
|
NM_001351736.1:c.629-926C>G
(RPUSD3)
|
NP_001338665.1:n.629-926C>G
|
|
NM_001351737.1:c.725-926C>G
(RPUSD3)
|
NP_001338666.1:n.725-926C>G
|
|
NM_001351738.1:c.791C>G
(RPUSD3)
|
NP_001338667.1:p.Ala264Gly
|
|
NM_173659.4:c.763C>G
(RPUSD3)
|
NP_775930.2:p.Leu255Val
|
|
XM_024453471.1:c.763C>G
(RPUSD3)
|
XP_024309239.1:p.Leu255Val
|
|
XM_024453472.1:c.724+1051C>G
(RPUSD3)
|
XP_024309240.1:n.724+1051C>G
|
|
NM_001351736.2:c.629-926C>G
(RPUSD3)
|
NP_001338665.1:n.629-926C>G
|
|
NM_001351736.3:c.629-926C>G
(RPUSD3)
|
NP_001338665.1:n.629-926C>G
|
|
NM_001142547.3:c.694C>G
(RPUSD3)
|
NP_001136019.2:p.Leu232Val
|
|
NM_001351737.2:c.701-926C>G
(RPUSD3)
|
NP_001338666.2:n.701-926C>G
|
|
NM_001351738.2:c.767C>G
(RPUSD3)
|
NP_001338667.2:p.Ala256Gly
|
|
NM_173659.5:c.739C>G
(RPUSD3)
MANE Select
|
NP_775930.3:p.Leu247Val
|
|