ENST00000342245.9:c.1721T>C
MANE Select
|
ENSP00000340409.4:p.Phe574Ser
|
|
ENST00000342245.8:c.1721T>C
|
ENSP00000340409.4:p.Phe574Ser
|
|
ENST00000526280.1:c.778T>C
|
|
|
ENST00000527275.5:c.1718T>C
|
ENSP00000435350.1:p.Phe573Ser
|
|
ENST00000531303.5:c.*572T>C
|
ENSP00000432625.1:n.*572T>C
|
|
ENST00000533123.5:c.*448T>C
|
ENSP00000435950.1:n.*448T>C
|
|
ENST00000534405.5:c.*552T>C
|
ENSP00000434353.1:n.*552T>C
|
|
NM_000543.4:c.1721T>C
|
NP_000534.3:p.Phe574Ser
|
|
NM_001007593.2:c.1718T>C
|
NP_001007594.2:p.Phe573Ser
|
|
XM_005253075.3:c.*214T>C
|
XP_005253132.1:n.*214T>C
|
|
XM_011520303.1:c.1589T>C
|
XP_011518605.1:p.Phe530Ser
|
|
XM_011520304.1:c.*214T>C
|
XP_011518606.1:n.*214T>C
|
|
NM_001318087.1:c.*214T>C
|
NP_001305016.1:n.*214T>C
|
|
NM_001318088.1:c.800T>C
|
NP_001305017.1:p.Phe267Ser
|
|
NM_001365135.1:c.1589T>C
|
NP_001352064.1:p.Phe530Ser
|
|
NR_027400.2:n.1734T>C
|
|
|
NR_134502.1:n.1273T>C
|
|
|
XM_011520304.2:c.*214T>C
|
XP_011518606.1:n.*214T>C
|
|
XR_001747940.2:n.1906T>C
|
|
|
XR_002957158.1:n.2088T>C
|
|
|
NM_000543.5:c.1721T>C
MANE Select
|
NP_000534.3:p.Phe574Ser
|
|
NM_001007593.3:c.1718T>C
|
NP_001007594.2:p.Phe573Ser
|
|
NM_001318087.2:c.*214T>C
|
NP_001305016.1:n.*214T>C
|
|
NM_001318088.2:c.800T>C
|
NP_001305017.1:p.Phe267Ser
|
|
NM_001365135.2:c.1589T>C
|
NP_001352064.1:p.Phe530Ser
|
|
NR_027400.3:n.1674T>C
|
|
|
NR_134502.2:n.1213T>C
|
|
|