|
NM_032119.4:c.6856C>T
MANE Select
|
NP_115495.3:p.Arg2286Ter
|
|
ENST00000405460.9:c.6856C>T
MANE Select
|
ENSP00000384582.2:p.Arg2286Ter
|
|
NM_032119.3:c.6856C>T
|
NP_115495.3:p.Arg2286Ter
|
|
NR_003149.1:n.6952C>T
|
|
|
NR_003149.2:n.6955C>T
|
|
|
ENST00000405460.6:c.6856C>T
|
ENSP00000384582.2:p.Arg2286Ter
|
|
ENST00000639431.1:c.265+14737C>T
|
ENSP00000491057.1:n.265+14737C>T
|
|
ENST00000639473.1:n.2315C>T
|
|
|
ENST00000640012.1:c.746C>T
|
|
|
ENST00000640403.1:c.4147C>T
|
ENSP00000492531.1:p.Arg1383Ter
|
|
ENST00000640779.1:c.1668C>T
|
|
|
XM_011543675.1:c.6853C>T
|
XP_011541977.1:p.Arg2285Ter
|
|
XM_011543676.1:c.6775C>T
|
XP_011541978.1:p.Arg2259Ter
|
|
XM_011543677.1:c.4159C>T
|
XP_011541979.1:p.Arg1387Ter
|
|
XM_011543678.1:c.6856C>T
|
XP_011541980.1:p.Arg2286Ter
|
|
XM_011543679.1:c.6856C>T
|
XP_011541981.1:p.Arg2286Ter
|
|
XM_017009963.2:c.6856C>T
|
XP_016865452.1:p.Arg2286Ter
|
|
XM_017009964.2:c.6853C>T
|
XP_016865453.1:p.Arg2285Ter
|
|
XM_017009965.1:c.6853C>T
|
XP_016865454.1:p.Arg2285Ter
|
|
XM_017009966.2:c.6775C>T
|
XP_016865455.1:p.Arg2259Ter
|
|
XM_017009967.1:c.6760C>T
|
XP_016865456.1:p.Arg2254Ter
|
|
XM_017009968.2:c.6856C>T
|
XP_016865457.1:p.Arg2286Ter
|
|
XM_017009969.2:c.6856C>T
|
XP_016865458.1:p.Arg2286Ter
|
|
XM_017009970.2:c.6856C>T
|
XP_016865459.1:p.Arg2286Ter
|
|
XM_017009971.2:c.6856C>T
|
XP_016865460.1:p.Arg2286Ter
|
|
XM_017009972.1:c.57C>T
|
XP_016865461.1:p.Cys19=
|
|
XM_017009973.1:c.57C>T
|
XP_016865462.1:p.Cys19=
|
|
XM_017009974.2:c.6856C>T
|
XP_016865463.1:p.Arg2286Ter
|