|
NM_032119.4:c.8892G>A
MANE Select
|
NP_115495.3:p.Trp2964Ter
|
|
ENST00000405460.9:c.8892G>A
MANE Select
|
ENSP00000384582.2:p.Trp2964Ter
|
|
NM_032119.3:c.8892G>A
|
NP_115495.3:p.Trp2964Ter
|
|
NR_003149.1:n.8905G>A
|
|
|
NR_003149.2:n.8908G>A
|
|
|
ENST00000405460.6:c.8892G>A
|
ENSP00000384582.2:p.Trp2964Ter
|
|
ENST00000509621.1:c.1589G>A
|
|
|
ENST00000639431.1:c.265+34839G>A
|
ENSP00000491057.1:n.265+34839G>A
|
|
ENST00000639473.1:n.4351G>A
|
|
|
ENST00000640012.1:c.2699G>A
|
|
|
ENST00000640374.1:n.2036G>A
|
|
|
ENST00000640779.1:c.3621G>A
|
|
|
XM_011543675.1:c.8889G>A
|
XP_011541977.1:p.Trp2963Ter
|
|
XM_011543676.1:c.8811G>A
|
XP_011541978.1:p.Trp2937Ter
|
|
XM_011543677.1:c.6195G>A
|
XP_011541979.1:p.Trp2065Ter
|
|
XM_011543678.1:c.8892G>A
|
XP_011541980.1:p.Trp2964Ter
|
|
XM_011543679.1:c.8892G>A
|
XP_011541981.1:p.Trp2964Ter
|
|
XM_017009963.2:c.8913G>A
|
XP_016865452.1:p.Trp2971Ter
|
|
XM_017009964.2:c.8910G>A
|
XP_016865453.1:p.Trp2970Ter
|
|
XM_017009965.1:c.8910G>A
|
XP_016865454.1:p.Trp2970Ter
|
|
XM_017009966.2:c.8832G>A
|
XP_016865455.1:p.Trp2944Ter
|
|
XM_017009967.1:c.8817G>A
|
XP_016865456.1:p.Trp2939Ter
|
|
XM_017009968.2:c.8913G>A
|
XP_016865457.1:p.Trp2971Ter
|
|
XM_017009969.2:c.8913G>A
|
XP_016865458.1:p.Trp2971Ter
|
|
XM_017009970.2:c.8913G>A
|
XP_016865459.1:p.Trp2971Ter
|
|
XM_017009971.2:c.8913G>A
|
XP_016865460.1:p.Trp2971Ter
|
|
XM_017009972.1:c.2031G>A
|
XP_016865461.1:p.Trp677Ter
|
|
XM_017009973.1:c.2010G>A
|
XP_016865462.1:p.Trp670Ter
|
|
XM_017009974.2:c.8913G>A
|
XP_016865463.1:p.Trp2971Ter
|