|
NM_032119.4:c.17258G>A
MANE Select
|
NP_115495.3:p.Trp5753Ter
|
|
ENST00000405460.9:c.17258G>A
MANE Select
|
ENSP00000384582.2:p.Trp5753Ter
|
|
NM_032119.3:c.17258G>A
|
NP_115495.3:p.Trp5753Ter
|
|
NR_003149.1:n.17271G>A
|
|
|
NR_003149.2:n.17274G>A
|
|
|
ENST00000405460.6:c.17258G>A
|
ENSP00000384582.2:p.Trp5753Ter
|
|
ENST00000425867.2:c.4241G>A
|
ENSP00000392618.2:p.Trp1414Ter
|
|
ENST00000425867.3:c.6212G>A
|
ENSP00000392618.3:p.Trp2071Ter
|
|
ENST00000505845.2:n.449G>A
|
|
|
ENST00000638510.1:n.4525G>A
|
|
|
ENST00000638990.1:c.470G>A
|
|
|
ENST00000639431.1:c.266-132007G>A
|
ENSP00000491057.1:n.266-132007G>A
|
|
ENST00000640407.1:c.3707G>A
|
ENSP00000491425.1:n.3707G>A
|
|
XM_011543675.1:c.17255G>A
|
XP_011541977.1:p.Trp5752Ter
|
|
XM_011543676.1:c.17177G>A
|
XP_011541978.1:p.Trp5726Ter
|
|
XM_011543677.1:c.14561G>A
|
XP_011541979.1:p.Trp4854Ter
|
|
XM_017009963.2:c.17279G>A
|
XP_016865452.1:p.Trp5760Ter
|
|
XM_017009964.2:c.17276G>A
|
XP_016865453.1:p.Trp5759Ter
|
|
XM_017009965.1:c.17276G>A
|
XP_016865454.1:p.Trp5759Ter
|
|
XM_017009966.2:c.17198G>A
|
XP_016865455.1:p.Trp5733Ter
|
|
XM_017009967.1:c.17183G>A
|
XP_016865456.1:p.Trp5728Ter
|
|
XM_017009968.2:c.17099G>A
|
XP_016865457.1:p.Trp5700Ter
|
|
XM_017009969.2:c.17279G>A
|
XP_016865458.1:p.Trp5760Ter
|
|
XM_017009972.1:c.10397G>A
|
XP_016865461.1:p.Trp3466Ter
|
|
XM_017009973.1:c.10376G>A
|
XP_016865462.1:p.Trp3459Ter
|