ENST00000342245.9:c.1891T>C
MANE Select
|
ENSP00000340409.4:p.Cys631Arg
|
|
ENST00000342245.8:c.1891T>C
|
ENSP00000340409.4:p.Cys631Arg
|
|
ENST00000526280.1:c.948T>C
|
|
|
ENST00000527275.5:c.1888T>C
|
ENSP00000435350.1:p.Cys630Arg
|
|
ENST00000531303.5:c.*742T>C
|
ENSP00000432625.1:n.*742T>C
|
|
ENST00000533123.5:c.*618T>C
|
ENSP00000435950.1:n.*618T>C
|
|
ENST00000534405.5:c.*722T>C
|
ENSP00000434353.1:n.*722T>C
|
|
NM_000543.4:c.1891T>C
|
NP_000534.3:p.Cys631Arg
|
|
NM_001007593.2:c.1888T>C
|
NP_001007594.2:p.Cys630Arg
|
|
XM_005253075.3:c.*384T>C
|
XP_005253132.1:n.*384T>C
|
|
XM_011520303.1:c.1759T>C
|
XP_011518605.1:p.Cys587Arg
|
|
NM_001318087.1:c.*384T>C
|
NP_001305016.1:n.*384T>C
|
|
NM_001318088.1:c.970T>C
|
NP_001305017.1:p.Cys324Arg
|
|
NM_001365135.1:c.1759T>C
|
NP_001352064.1:p.Cys587Arg
|
|
NR_027400.2:n.1904T>C
|
|
|
NR_134502.1:n.1443T>C
|
|
|
XR_001747940.2:n.2076T>C
|
|
|
XR_002957158.1:n.2258T>C
|
|
|
NM_000543.5:c.1891T>C
MANE Select
|
NP_000534.3:p.Cys631Arg
|
|
NM_001007593.3:c.1888T>C
|
NP_001007594.2:p.Cys630Arg
|
|
NM_001318087.2:c.*384T>C
|
NP_001305016.1:n.*384T>C
|
|
NM_001318088.2:c.970T>C
|
NP_001305017.1:p.Cys324Arg
|
|
NM_001365135.2:c.1759T>C
|
NP_001352064.1:p.Cys587Arg
|
|
NR_027400.3:n.1844T>C
|
|
|
NR_134502.2:n.1383T>C
|
|
|