ENST00000342245.9:c.1768T>C
MANE Select
|
ENSP00000340409.4:p.Cys590Arg
|
|
ENST00000342245.8:c.1768T>C
|
ENSP00000340409.4:p.Cys590Arg
|
|
ENST00000526280.1:c.825T>C
|
|
|
ENST00000527275.5:c.1765T>C
|
ENSP00000435350.1:p.Cys589Arg
|
|
ENST00000531303.5:c.*619T>C
|
ENSP00000432625.1:n.*619T>C
|
|
ENST00000533123.5:c.*495T>C
|
ENSP00000435950.1:n.*495T>C
|
|
ENST00000534405.5:c.*599T>C
|
ENSP00000434353.1:n.*599T>C
|
|
NM_000543.4:c.1768T>C
|
NP_000534.3:p.Cys590Arg
|
|
NM_001007593.2:c.1765T>C
|
NP_001007594.2:p.Cys589Arg
|
|
XM_005253075.3:c.*261T>C
|
XP_005253132.1:n.*261T>C
|
|
XM_011520303.1:c.1636T>C
|
XP_011518605.1:p.Cys546Arg
|
|
XM_011520304.1:c.*261T>C
|
XP_011518606.1:n.*261T>C
|
|
NM_001318087.1:c.*261T>C
|
NP_001305016.1:n.*261T>C
|
|
NM_001318088.1:c.847T>C
|
NP_001305017.1:p.Cys283Arg
|
|
NM_001365135.1:c.1636T>C
|
NP_001352064.1:p.Cys546Arg
|
|
NR_027400.2:n.1781T>C
|
|
|
NR_134502.1:n.1320T>C
|
|
|
XM_011520304.2:c.*261T>C
|
XP_011518606.1:n.*261T>C
|
|
XR_001747940.2:n.1953T>C
|
|
|
XR_002957158.1:n.2135T>C
|
|
|
NM_000543.5:c.1768T>C
MANE Select
|
NP_000534.3:p.Cys590Arg
|
|
NM_001007593.3:c.1765T>C
|
NP_001007594.2:p.Cys589Arg
|
|
NM_001318087.2:c.*261T>C
|
NP_001305016.1:n.*261T>C
|
|
NM_001318088.2:c.847T>C
|
NP_001305017.1:p.Cys283Arg
|
|
NM_001365135.2:c.1636T>C
|
NP_001352064.1:p.Cys546Arg
|
|
NR_027400.3:n.1721T>C
|
|
|
NR_134502.2:n.1260T>C
|
|
|