ENST00000405460.9:c.16347C>A
MANE Select
|
ENSP00000384582.2:p.Ser5449Arg
|
|
ENST00000425867.3:c.5301C>A
|
ENSP00000392618.3:p.Ser1767Arg
|
|
ENST00000638510.1:n.3614C>A
|
|
|
ENST00000639431.1:c.265+147366C>A
|
ENSP00000491057.1:n.265+147366C>A
|
|
ENST00000640061.1:n.128+1393C>A
|
|
|
ENST00000640407.1:c.2757C>A
|
ENSP00000491425.1:p.Ser919Arg
|
|
ENST00000405460.6:c.16347C>A
|
ENSP00000384582.2:p.Ser5449Arg
|
|
ENST00000425867.2:c.3330C>A
|
ENSP00000392618.2:p.Ser1110Arg
|
|
NM_032119.3:c.16347C>A
|
NP_115495.3:p.Ser5449Arg
|
|
NR_003149.1:n.16360C>A
|
|
|
XM_011543675.1:c.16344C>A
|
XP_011541977.1:p.Ser5448Arg
|
|
XM_011543676.1:c.16266C>A
|
XP_011541978.1:p.Ser5422Arg
|
|
XM_011543677.1:c.13650C>A
|
XP_011541979.1:p.Ser4550Arg
|
|
NM_032119.4:c.16347C>A
MANE Select
|
NP_115495.3:p.Ser5449Arg
|
|
XM_017009963.2:c.16368C>A
|
XP_016865452.1:p.Ser5456Arg
|
|
XM_017009964.2:c.16365C>A
|
XP_016865453.1:p.Ser5455Arg
|
|
XM_017009965.1:c.16365C>A
|
XP_016865454.1:p.Ser5455Arg
|
|
XM_017009966.2:c.16287C>A
|
XP_016865455.1:p.Ser5429Arg
|
|
XM_017009967.1:c.16272C>A
|
XP_016865456.1:p.Ser5424Arg
|
|
XM_017009968.2:c.16188C>A
|
XP_016865457.1:p.Ser5396Arg
|
|
XM_017009969.2:c.16368C>A
|
XP_016865458.1:p.Ser5456Arg
|
|
XM_017009972.1:c.9486C>A
|
XP_016865461.1:p.Ser3162Arg
|
|
XM_017009973.1:c.9465C>A
|
XP_016865462.1:p.Ser3155Arg
|
|
NR_003149.2:n.16363C>A
|
|
|