ENST00000293195.10:c.916C>T
MANE Select
|
ENSP00000293195.5:p.Arg306Cys
|
|
ENST00000293195.9:c.916C>T
|
ENSP00000293195.5:p.Arg306Cys
|
|
ENST00000413947.6:c.1009C>T
|
ENSP00000408595.2:p.Arg337Cys
|
|
ENST00000420580.6:c.796C>T
|
ENSP00000414172.2:p.Arg266Cys
|
|
ENST00000442102.6:c.1045C>T
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ENSP00000416515.2:p.Arg349Cys
|
|
ENST00000544854.5:c.760C>T
|
ENSP00000445432.1:p.Arg254Cys
|
|
ENST00000577509.5:c.*875C>T
|
ENSP00000462083.1:n.*875C>T
|
|
ENST00000578473.5:n.1604C>T
|
|
|
ENST00000579482.5:c.*1028C>T
|
ENSP00000461993.1:n.*1028C>T
|
|
ENST00000581530.5:c.934C>T
|
ENSP00000462972.1:p.Arg312Cys
|
|
ENST00000582944.5:c.892C>T
|
ENSP00000462183.1:p.Arg298Cys
|
|
ENST00000583881.5:c.*553C>T
|
ENSP00000464670.1:n.*553C>T
|
|
ENST00000583917.5:c.832C>T
|
ENSP00000463940.1:p.Arg278Cys
|
|
NM_001258012.3:c.1045C>T
|
NP_001244941.2:p.Arg349Cys
|
|
NM_001258013.3:c.1009C>T
|
NP_001244942.2:p.Arg337Cys
|
|
NM_001258014.3:c.892C>T
|
NP_001244943.2:p.Arg298Cys
|
|
NM_001258015.2:c.796C>T
|
NP_001244944.1:p.Arg266Cys
|
|
NM_001258016.3:c.760C>T
|
NP_001244945.2:p.Arg254Cys
|
|
NM_004110.5:c.934C>T
|
NP_004101.3:p.Arg312Cys
|
|
NM_024417.4:c.916C>T
|
NP_077728.3:p.Arg306Cys
|
|
NR_047576.2:n.1103C>T
|
|
|
XM_006721772.1:c.919C>T
|
XP_006721835.1:p.Arg307Cys
|
|
XM_011524527.1:c.937C>T
|
XP_011522829.1:p.Arg313Cys
|
|
XM_011524528.1:c.928C>T
|
XP_011522830.1:p.Arg310Cys
|
|
XM_011524529.1:c.925C>T
|
XP_011522831.1:p.Arg309Cys
|
|
XM_011524530.1:c.799C>T
|
XP_011522832.1:p.Arg267Cys
|
|
XM_011524531.1:c.781C>T
|
XP_011522833.1:p.Arg261Cys
|
|
XM_011524532.1:c.778C>T
|
XP_011522834.1:p.Arg260Cys
|
|
XM_011524533.1:c.763C>T
|
XP_011522835.1:p.Arg255Cys
|
|
XM_006721772.2:c.919C>T
|
XP_006721835.1:p.Arg307Cys
|
|
XM_011524527.2:c.937C>T
|
XP_011522829.1:p.Arg313Cys
|
|
XM_011524531.2:c.781C>T
|
XP_011522833.1:p.Arg261Cys
|
|
XM_011524532.2:c.778C>T
|
XP_011522834.1:p.Arg260Cys
|
|
XM_011524533.2:c.763C>T
|
XP_011522835.1:p.Arg255Cys
|
|
XM_024450648.1:c.634C>T
|
XP_024306416.1:p.Arg212Cys
|
|
XM_024450649.1:c.187C>T
|
XP_024306417.1:p.Arg63Cys
|
|
XM_024450650.1:c.187C>T
|
XP_024306418.1:p.Arg63Cys
|
|
XR_002957983.1:n.1043C>T
|
|
|
NM_024417.5:c.916C>T
MANE Select
|
NP_077728.3:p.Arg306Cys
|
|
NM_001258012.4:c.1045C>T
|
NP_001244941.2:p.Arg349Cys
|
|
NM_001258013.4:c.1009C>T
|
NP_001244942.2:p.Arg337Cys
|
|
NM_001258014.4:c.892C>T
|
NP_001244943.2:p.Arg298Cys
|
|
NM_001258015.3:c.796C>T
|
NP_001244944.1:p.Arg266Cys
|
|
NM_004110.6:c.934C>T
|
NP_004101.3:p.Arg312Cys
|
|
NR_047576.3:n.1066C>T
|
|
|