|
NM_032119.4:c.11339G>A
MANE Select
|
NP_115495.3:p.Arg3780His
|
|
ENST00000405460.9:c.11339G>A
MANE Select
|
ENSP00000384582.2:p.Arg3780His
|
|
NM_032119.3:c.11339G>A
|
NP_115495.3:p.Arg3780His
|
|
NR_003149.1:n.11352G>A
|
|
|
NR_003149.2:n.11355G>A
|
|
|
ENST00000405460.6:c.11339G>A
|
ENSP00000384582.2:p.Arg3780His
|
|
ENST00000425867.3:c.470G>A
|
ENSP00000392618.3:p.Arg157His
|
|
ENST00000509621.1:c.4036G>A
|
|
|
ENST00000639431.1:c.265+77582G>A
|
ENSP00000491057.1:n.265+77582G>A
|
|
ENST00000640374.1:n.4483G>A
|
|
|
ENST00000640464.1:n.1758G>A
|
|
|
XM_011543675.1:c.11336G>A
|
XP_011541977.1:p.Arg3779His
|
|
XM_011543676.1:c.11258G>A
|
XP_011541978.1:p.Arg3753His
|
|
XM_011543677.1:c.8642G>A
|
XP_011541979.1:p.Arg2881His
|
|
XM_011543678.1:c.11339G>A
|
XP_011541980.1:p.Arg3780His
|
|
XM_017009963.2:c.11360G>A
|
XP_016865452.1:p.Arg3787His
|
|
XM_017009964.2:c.11357G>A
|
XP_016865453.1:p.Arg3786His
|
|
XM_017009965.1:c.11357G>A
|
XP_016865454.1:p.Arg3786His
|
|
XM_017009966.2:c.11279G>A
|
XP_016865455.1:p.Arg3760His
|
|
XM_017009967.1:c.11264G>A
|
XP_016865456.1:p.Arg3755His
|
|
XM_017009968.2:c.11360G>A
|
XP_016865457.1:p.Arg3787His
|
|
XM_017009969.2:c.11360G>A
|
XP_016865458.1:p.Arg3787His
|
|
XM_017009970.2:c.11360G>A
|
XP_016865459.1:p.Arg3787His
|
|
XM_017009971.2:c.11360G>A
|
XP_016865460.1:p.Arg3787His
|
|
XM_017009972.1:c.4478G>A
|
XP_016865461.1:p.Arg1493His
|
|
XM_017009973.1:c.4457G>A
|
XP_016865462.1:p.Arg1486His
|