|
NM_032119.4:c.12895C>T
MANE Select
|
NP_115495.3:p.Arg4299Ter
|
|
ENST00000405460.9:c.12895C>T
MANE Select
|
ENSP00000384582.2:p.Arg4299Ter
|
|
NM_032119.3:c.12895C>T
|
NP_115495.3:p.Arg4299Ter
|
|
NR_003149.1:n.12908C>T
|
|
|
NR_003149.2:n.12911C>T
|
|
|
ENST00000405460.6:c.12895C>T
|
ENSP00000384582.2:p.Arg4299Ter
|
|
ENST00000425867.3:c.1849C>T
|
ENSP00000392618.3:p.Arg617Ter
|
|
ENST00000639431.1:c.265+102701C>T
|
ENSP00000491057.1:n.265+102701C>T
|
|
ENST00000640464.1:n.3314C>T
|
|
|
XM_011543675.1:c.12892C>T
|
XP_011541977.1:p.Arg4298Ter
|
|
XM_011543676.1:c.12814C>T
|
XP_011541978.1:p.Arg4272Ter
|
|
XM_011543677.1:c.10198C>T
|
XP_011541979.1:p.Arg3400Ter
|
|
XM_011543678.1:c.12895C>T
|
XP_011541980.1:p.Arg4299Ter
|
|
XM_017009963.2:c.12916C>T
|
XP_016865452.1:p.Arg4306Ter
|
|
XM_017009964.2:c.12913C>T
|
XP_016865453.1:p.Arg4305Ter
|
|
XM_017009965.1:c.12913C>T
|
XP_016865454.1:p.Arg4305Ter
|
|
XM_017009966.2:c.12835C>T
|
XP_016865455.1:p.Arg4279Ter
|
|
XM_017009967.1:c.12820C>T
|
XP_016865456.1:p.Arg4274Ter
|
|
XM_017009968.2:c.12916C>T
|
XP_016865457.1:p.Arg4306Ter
|
|
XM_017009969.2:c.12916C>T
|
XP_016865458.1:p.Arg4306Ter
|
|
XM_017009970.2:c.12916C>T
|
XP_016865459.1:p.Arg4306Ter
|
|
XM_017009971.2:c.12916C>T
|
XP_016865460.1:p.Arg4306Ter
|
|
XM_017009972.1:c.6034C>T
|
XP_016865461.1:p.Arg2012Ter
|
|
XM_017009973.1:c.6013C>T
|
XP_016865462.1:p.Arg2005Ter
|