ENST00000372492.9:c.1543-46T>C
(CFAP57)
MANE Select
|
ENSP00000361570.4:n.1543-46T>C
|
|
ENST00000372492.8:c.1543-46T>C
(CFAP57)
|
ENSP00000361570.4:n.1543-46T>C
|
|
ENST00000461557.2:n.233+4776A>G
(EBNA1BP2)
|
|
|
ENST00000466927.5:n.197+8592A>G
(EBNA1BP2)
|
|
|
ENST00000474566.1:n.420-282A>G
(EBNA1BP2)
|
|
|
ENST00000528956.5:c.1543-46T>C
(CFAP57)
|
ENSP00000435310.1:n.1543-46T>C
|
|
ENST00000533339.1:c.*1442-46T>C
(CFAP57)
|
ENSP00000432547.1:n.*1442-46T>C
|
|
ENST00000610710.4:c.1543-46T>C
(CFAP57)
|
ENSP00000479773.1:n.1543-46T>C
|
|
NM_001167965.1:c.1543-46T>C
(CFAP57)
|
NP_001161437.1:n.1543-46T>C
|
|
NM_001195831.2:c.1543-46T>C
(CFAP57)
|
NP_001182760.2:n.1543-46T>C
|
|
NM_152498.3:c.1543-46T>C
(CFAP57)
|
NP_689711.2:n.1543-46T>C
|
|
XM_005270520.1:c.1543-46T>C
(CFAP57)
|
XP_005270577.1:n.1543-46T>C
|
|
XM_006710383.1:c.1510-46T>C
(CFAP57)
|
XP_006710446.1:n.1510-46T>C
|
|
XM_011540793.1:c.1543-46T>C
(CFAP57)
|
XP_011539095.1:n.1543-46T>C
|
|
XM_011540794.1:c.1543-46T>C
(CFAP57)
|
XP_011539096.1:n.1543-46T>C
|
|
XM_011540795.1:c.1543-46T>C
(CFAP57)
|
XP_011539097.1:n.1543-46T>C
|
|
XM_011540796.1:c.1510-46T>C
(CFAP57)
|
XP_011539098.1:n.1510-46T>C
|
|
XM_011540797.1:c.1480-46T>C
(CFAP57)
|
XP_011539099.1:n.1480-46T>C
|
|
XM_011540798.1:c.1543-3069T>C
(CFAP57)
|
XP_011539100.1:n.1543-3069T>C
|
|
XM_011540799.1:c.1542+7171T>C
(CFAP57)
|
XP_011539101.1:n.1542+7171T>C
|
|
XM_011540800.1:c.1543-46T>C
(CFAP57)
|
XP_011539102.1:n.1543-46T>C
|
|
XM_011540801.1:c.1543-46T>C
(CFAP57)
|
XP_011539103.1:n.1543-46T>C
|
|
XR_947266.1:n.450-282A>G
|
|
|
XR_947267.1:n.455-282A>G
|
|
|
XR_947268.1:n.240-282A>G
|
|
|
XR_947269.1:n.1064-282A>G
|
|
|
XR_947270.1:n.214-282A>G
|
|
|
XR_947271.1:n.885-282A>G
|
|
|
XR_947273.1:n.448+8592A>G
|
|
|
XR_947274.1:n.453-282A>G
|
|
|
XM_005270520.2:c.1543-46T>C
(CFAP57)
|
XP_005270577.1:n.1543-46T>C
|
|
XM_011540795.3:c.1543-46T>C
(CFAP57)
|
XP_011539097.1:n.1543-46T>C
|
|
XM_011540797.2:c.1480-46T>C
(CFAP57)
|
XP_011539099.1:n.1480-46T>C
|
|
XM_011540800.2:c.1543-46T>C
(CFAP57)
|
XP_011539102.1:n.1543-46T>C
|
|
XM_017000421.1:c.1543-46T>C
(CFAP57)
|
XP_016855910.1:n.1543-46T>C
|
|
XM_017000422.2:c.1543-46T>C
(CFAP57)
|
XP_016855911.1:n.1543-46T>C
|
|
XR_001736994.2:n.1672-46T>C
(CFAP57)
|
|
|
XR_001738021.1:n.532-282A>G
|
|
|
XR_001738022.1:n.529-282A>G
|
|
|
XR_001738023.2:n.827-282A>G
|
|
|
XR_001738024.1:n.539+8592A>G
|
|
|
XR_947266.2:n.521-282A>G
|
|
|
XR_947268.2:n.247-282A>G
|
|
|
XR_947271.2:n.888-282A>G
|
|
|
XR_947273.2:n.538+8592A>G
|
|
|
XR_947274.2:n.827-282A>G
|
|
|
NM_001195831.3:c.1543-46T>C
(CFAP57)
|
NP_001182760.2:n.1543-46T>C
|
|
NM_001378189.1:c.1543-46T>C
(CFAP57)
MANE Select
|
NP_001365118.1:n.1543-46T>C
|
|