|
NM_032119.4:c.11338C>T
MANE Select
|
NP_115495.3:p.Arg3780Cys
|
|
ENST00000405460.9:c.11338C>T
MANE Select
|
ENSP00000384582.2:p.Arg3780Cys
|
|
NM_032119.3:c.11338C>T
|
NP_115495.3:p.Arg3780Cys
|
|
NR_003149.1:n.11351C>T
|
|
|
NR_003149.2:n.11354C>T
|
|
|
ENST00000405460.6:c.11338C>T
|
ENSP00000384582.2:p.Arg3780Cys
|
|
ENST00000425867.3:c.469C>T
|
ENSP00000392618.3:p.Arg157Cys
|
|
ENST00000509621.1:c.4035C>T
|
|
|
ENST00000639431.1:c.265+77581C>T
|
ENSP00000491057.1:n.265+77581C>T
|
|
ENST00000640374.1:n.4482C>T
|
|
|
ENST00000640464.1:n.1757C>T
|
|
|
XM_011543675.1:c.11335C>T
|
XP_011541977.1:p.Arg3779Cys
|
|
XM_011543676.1:c.11257C>T
|
XP_011541978.1:p.Arg3753Cys
|
|
XM_011543677.1:c.8641C>T
|
XP_011541979.1:p.Arg2881Cys
|
|
XM_011543678.1:c.11338C>T
|
XP_011541980.1:p.Arg3780Cys
|
|
XM_017009963.2:c.11359C>T
|
XP_016865452.1:p.Arg3787Cys
|
|
XM_017009964.2:c.11356C>T
|
XP_016865453.1:p.Arg3786Cys
|
|
XM_017009965.1:c.11356C>T
|
XP_016865454.1:p.Arg3786Cys
|
|
XM_017009966.2:c.11278C>T
|
XP_016865455.1:p.Arg3760Cys
|
|
XM_017009967.1:c.11263C>T
|
XP_016865456.1:p.Arg3755Cys
|
|
XM_017009968.2:c.11359C>T
|
XP_016865457.1:p.Arg3787Cys
|
|
XM_017009969.2:c.11359C>T
|
XP_016865458.1:p.Arg3787Cys
|
|
XM_017009970.2:c.11359C>T
|
XP_016865459.1:p.Arg3787Cys
|
|
XM_017009971.2:c.11359C>T
|
XP_016865460.1:p.Arg3787Cys
|
|
XM_017009972.1:c.4477C>T
|
XP_016865461.1:p.Arg1493Cys
|
|
XM_017009973.1:c.4456C>T
|
XP_016865462.1:p.Arg1486Cys
|