ENST00000342245.9:c.1160G>T
MANE Select
|
ENSP00000340409.4:p.Cys387Phe
|
|
ENST00000342245.8:c.1160G>T
|
ENSP00000340409.4:p.Cys387Phe
|
|
ENST00000526280.1:c.321-333G>T
|
|
|
ENST00000527275.5:c.1157G>T
|
ENSP00000435350.1:p.Cys386Phe
|
|
ENST00000531303.5:c.507G>T
|
ENSP00000432625.1:p.Leu169Phe
|
|
ENST00000533123.5:c.1092-333G>T
|
ENSP00000435950.1:n.1092-333G>T
|
|
ENST00000534405.5:c.1200G>T
|
ENSP00000434353.1:p.Leu400Phe
|
|
NM_000543.4:c.1160G>T
|
NP_000534.3:p.Cys387Phe
|
|
NM_001007593.2:c.1157G>T
|
NP_001007594.2:p.Cys386Phe
|
|
XM_005253075.3:c.1160G>T
|
XP_005253132.1:p.Cys387Phe
|
|
XM_011520303.1:c.1132-333G>T
|
XP_011518605.1:n.1132-333G>T
|
|
XM_011520304.1:c.1132-333G>T
|
XP_011518606.1:n.1132-333G>T
|
|
XR_930886.1:n.1498G>T
|
|
|
NM_001318087.1:c.1160G>T
|
NP_001305016.1:p.Cys387Phe
|
|
NM_001318088.1:c.239G>T
|
NP_001305017.1:p.Cys80Phe
|
|
NM_001365135.1:c.1132-333G>T
|
NP_001352064.1:n.1132-333G>T
|
|
NR_027400.2:n.1277-333G>T
|
|
|
NR_134502.1:n.692G>T
|
|
|
XM_011520304.2:c.1132-333G>T
|
XP_011518606.1:n.1132-333G>T
|
|
XR_001747940.2:n.1325G>T
|
|
|
XR_002957158.1:n.1325G>T
|
|
|
NM_000543.5:c.1160G>T
MANE Select
|
NP_000534.3:p.Cys387Phe
|
|
NM_001007593.3:c.1157G>T
|
NP_001007594.2:p.Cys386Phe
|
|
NM_001318087.2:c.1160G>T
|
NP_001305016.1:p.Cys387Phe
|
|
NM_001318088.2:c.239G>T
|
NP_001305017.1:p.Cys80Phe
|
|
NM_001365135.2:c.1132-333G>T
|
NP_001352064.1:n.1132-333G>T
|
|
NR_027400.3:n.1217-333G>T
|
|
|
NR_134502.2:n.632G>T
|
|
|