ENST00000405460.9:c.11558A>G
MANE Select
|
ENSP00000384582.2:p.His3853Arg
|
|
ENST00000425867.3:c.689A>G
|
ENSP00000392618.3:p.His230Arg
|
|
ENST00000639431.1:c.265+78954A>G
|
ENSP00000491057.1:n.265+78954A>G
|
|
ENST00000640374.1:n.4702A>G
|
|
|
ENST00000640464.1:n.1977A>G
|
|
|
ENST00000405460.6:c.11558A>G
|
ENSP00000384582.2:p.His3853Arg
|
|
ENST00000509621.1:c.4255A>G
|
|
|
NM_032119.3:c.11558A>G
|
NP_115495.3:p.His3853Arg
|
|
NR_003149.1:n.11571A>G
|
|
|
XM_011543675.1:c.11555A>G
|
XP_011541977.1:p.His3852Arg
|
|
XM_011543676.1:c.11477A>G
|
XP_011541978.1:p.His3826Arg
|
|
XM_011543677.1:c.8861A>G
|
XP_011541979.1:p.His2954Arg
|
|
XM_011543678.1:c.11558A>G
|
XP_011541980.1:p.His3853Arg
|
|
NM_032119.4:c.11558A>G
MANE Select
|
NP_115495.3:p.His3853Arg
|
|
XM_017009963.2:c.11579A>G
|
XP_016865452.1:p.His3860Arg
|
|
XM_017009964.2:c.11576A>G
|
XP_016865453.1:p.His3859Arg
|
|
XM_017009965.1:c.11576A>G
|
XP_016865454.1:p.His3859Arg
|
|
XM_017009966.2:c.11498A>G
|
XP_016865455.1:p.His3833Arg
|
|
XM_017009967.1:c.11483A>G
|
XP_016865456.1:p.His3828Arg
|
|
XM_017009968.2:c.11579A>G
|
XP_016865457.1:p.His3860Arg
|
|
XM_017009969.2:c.11579A>G
|
XP_016865458.1:p.His3860Arg
|
|
XM_017009970.2:c.11579A>G
|
XP_016865459.1:p.His3860Arg
|
|
XM_017009971.2:c.11579A>G
|
XP_016865460.1:p.His3860Arg
|
|
XM_017009972.1:c.4697A>G
|
XP_016865461.1:p.His1566Arg
|
|
XM_017009973.1:c.4676A>G
|
XP_016865462.1:p.His1559Arg
|
|
NR_003149.2:n.11574A>G
|
|
|