|
NM_032119.4:c.17200G>T
MANE Select
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NP_115495.3:p.Glu5734Ter
|
|
ENST00000405460.9:c.17200G>T
MANE Select
|
ENSP00000384582.2:p.Glu5734Ter
|
|
NM_032119.3:c.17200G>T
|
NP_115495.3:p.Glu5734Ter
|
|
NR_003149.1:n.17213G>T
|
|
|
NR_003149.2:n.17216G>T
|
|
|
ENST00000405460.6:c.17200G>T
|
ENSP00000384582.2:p.Glu5734Ter
|
|
ENST00000425867.2:c.4183G>T
|
ENSP00000392618.2:p.Glu1395Ter
|
|
ENST00000425867.3:c.6154G>T
|
ENSP00000392618.3:p.Glu2052Ter
|
|
ENST00000505845.1:n.391G>T
|
|
|
ENST00000505845.2:n.391G>T
|
|
|
ENST00000638510.1:n.4467G>T
|
|
|
ENST00000638990.1:c.221G>T
|
|
|
ENST00000639431.1:c.266-136527G>T
|
ENSP00000491057.1:n.266-136527G>T
|
|
ENST00000640407.1:c.3649G>T
|
ENSP00000491425.1:n.3649G>T
|
|
XM_011543675.1:c.17197G>T
|
XP_011541977.1:p.Glu5733Ter
|
|
XM_011543676.1:c.17119G>T
|
XP_011541978.1:p.Glu5707Ter
|
|
XM_011543677.1:c.14503G>T
|
XP_011541979.1:p.Glu4835Ter
|
|
XM_017009963.2:c.17221G>T
|
XP_016865452.1:p.Glu5741Ter
|
|
XM_017009964.2:c.17218G>T
|
XP_016865453.1:p.Glu5740Ter
|
|
XM_017009965.1:c.17218G>T
|
XP_016865454.1:p.Glu5740Ter
|
|
XM_017009966.2:c.17140G>T
|
XP_016865455.1:p.Glu5714Ter
|
|
XM_017009967.1:c.17125G>T
|
XP_016865456.1:p.Glu5709Ter
|
|
XM_017009968.2:c.17041G>T
|
XP_016865457.1:p.Glu5681Ter
|
|
XM_017009969.2:c.17221G>T
|
XP_016865458.1:p.Glu5741Ter
|
|
XM_017009972.1:c.10339G>T
|
XP_016865461.1:p.Glu3447Ter
|
|
XM_017009973.1:c.10318G>T
|
XP_016865462.1:p.Glu3440Ter
|