ENST00000342245.9:c.1528T>A
MANE Select
|
ENSP00000340409.4:p.Ser510Thr
|
|
ENST00000342245.8:c.1528T>A
|
ENSP00000340409.4:p.Ser510Thr
|
|
ENST00000526280.1:c.585T>A
|
|
|
ENST00000527275.5:c.1525T>A
|
ENSP00000435350.1:p.Ser509Thr
|
|
ENST00000531303.5:c.*379T>A
|
ENSP00000432625.1:n.*379T>A
|
|
ENST00000531336.1:n.516T>A
|
|
|
ENST00000533123.5:c.*255T>A
|
ENSP00000435950.1:n.*255T>A
|
|
ENST00000534405.5:c.*359T>A
|
ENSP00000434353.1:n.*359T>A
|
|
NM_000543.4:c.1528T>A
|
NP_000534.3:p.Ser510Thr
|
|
NM_001007593.2:c.1525T>A
|
NP_001007594.2:p.Ser509Thr
|
|
XM_005253075.3:c.*21T>A
|
XP_005253132.1:n.*21T>A
|
|
XM_011520303.1:c.1396T>A
|
XP_011518605.1:p.Ser466Thr
|
|
XM_011520304.1:c.*21T>A
|
XP_011518606.1:n.*21T>A
|
|
NM_001318087.1:c.*21T>A
|
NP_001305016.1:n.*21T>A
|
|
NM_001318088.1:c.607T>A
|
NP_001305017.1:p.Ser203Thr
|
|
NM_001365135.1:c.1396T>A
|
NP_001352064.1:p.Ser466Thr
|
|
NR_027400.2:n.1541T>A
|
|
|
NR_134502.1:n.1080T>A
|
|
|
XM_011520304.2:c.*21T>A
|
XP_011518606.1:n.*21T>A
|
|
XR_001747940.2:n.1713T>A
|
|
|
XR_002957158.1:n.1895T>A
|
|
|
NM_000543.5:c.1528T>A
MANE Select
|
NP_000534.3:p.Ser510Thr
|
|
NM_001007593.3:c.1525T>A
|
NP_001007594.2:p.Ser509Thr
|
|
NM_001318087.2:c.*21T>A
|
NP_001305016.1:n.*21T>A
|
|
NM_001318088.2:c.607T>A
|
NP_001305017.1:p.Ser203Thr
|
|
NM_001365135.2:c.1396T>A
|
NP_001352064.1:p.Ser466Thr
|
|
NR_027400.3:n.1481T>A
|
|
|
NR_134502.2:n.1020T>A
|
|
|