ENST00000383820.10:c.766T>C
(RPUSD3)
MANE Select
|
ENSP00000373331.6:p.Tyr256His
|
|
ENST00000433535.7:c.721T>C
(RPUSD3)
|
ENSP00000398921.3:p.Tyr241His
|
|
ENST00000383820.9:c.790T>C
(RPUSD3)
|
ENSP00000373331.5:p.Tyr264His
|
|
ENST00000423108.5:c.276T>C
(RPUSD3)
|
|
|
ENST00000424438.5:c.629-899T>C
(RPUSD3)
|
ENSP00000408693.1:n.629-899T>C
|
|
ENST00000427174.5:c.790T>C
(RPUSD3)
|
|
|
ENST00000433535.6:c.745T>C
(RPUSD3)
|
ENSP00000398921.2:p.Tyr249His
|
|
ENST00000455274.5:c.918+9711A>G
(TTLL3)
|
ENSP00000409632.1:n.918+9711A>G
|
|
ENST00000464783.1:n.749T>C
(RPUSD3)
|
|
|
ENST00000466141.1:n.608T>C
(RPUSD3)
|
|
|
NM_001142547.1:c.745T>C
(RPUSD3)
|
NP_001136019.1:p.Tyr249His
|
|
NM_173659.3:c.790T>C
(RPUSD3)
|
NP_775930.2:p.Tyr264His
|
|
XM_011533627.1:c.725-899T>C
(RPUSD3)
|
XP_011531929.1:n.725-899T>C
|
|
NM_001142547.2:c.745T>C
(RPUSD3)
|
NP_001136019.1:p.Tyr249His
|
|
NM_001351736.1:c.629-899T>C
(RPUSD3)
|
NP_001338665.1:n.629-899T>C
|
|
NM_001351737.1:c.725-899T>C
(RPUSD3)
|
NP_001338666.1:n.725-899T>C
|
|
NM_001351738.1:c.818T>C
(RPUSD3)
|
NP_001338667.1:p.Val273Ala
|
|
NM_173659.4:c.790T>C
(RPUSD3)
|
NP_775930.2:p.Tyr264His
|
|
XM_024453471.1:c.790T>C
(RPUSD3)
|
XP_024309239.1:p.Tyr264His
|
|
XM_024453472.1:c.724+1078T>C
(RPUSD3)
|
XP_024309240.1:n.724+1078T>C
|
|
NM_001351736.2:c.629-899T>C
(RPUSD3)
|
NP_001338665.1:n.629-899T>C
|
|
NM_001351736.3:c.629-899T>C
(RPUSD3)
|
NP_001338665.1:n.629-899T>C
|
|
NM_001142547.3:c.721T>C
(RPUSD3)
|
NP_001136019.2:p.Tyr241His
|
|
NM_001351737.2:c.701-899T>C
(RPUSD3)
|
NP_001338666.2:n.701-899T>C
|
|
NM_001351738.2:c.794T>C
(RPUSD3)
|
NP_001338667.2:p.Val265Ala
|
|
NM_173659.5:c.766T>C
(RPUSD3)
MANE Select
|
NP_775930.3:p.Tyr256His
|
|