|
NM_032119.4:c.13460T>A
MANE Select
|
NP_115495.3:p.Leu4487Gln
|
|
ENST00000405460.9:c.13460T>A
MANE Select
|
ENSP00000384582.2:p.Leu4487Gln
|
|
NM_032119.3:c.13460T>A
|
NP_115495.3:p.Leu4487Gln
|
|
NR_003149.1:n.13473T>A
|
|
|
NR_003149.2:n.13476T>A
|
|
|
ENST00000405460.6:c.13460T>A
|
ENSP00000384582.2:p.Leu4487Gln
|
|
ENST00000425867.2:c.443T>A
|
ENSP00000392618.2:p.Leu148Gln
|
|
ENST00000425867.3:c.2414T>A
|
ENSP00000392618.3:p.Leu805Gln
|
|
ENST00000638510.1:n.727T>A
|
|
|
ENST00000638975.1:c.89T>A
|
ENSP00000492630.1:p.Leu30Gln
|
|
ENST00000639431.1:c.265+107655T>A
|
ENSP00000491057.1:n.265+107655T>A
|
|
XM_011543675.1:c.13457T>A
|
XP_011541977.1:p.Leu4486Gln
|
|
XM_011543676.1:c.13379T>A
|
XP_011541978.1:p.Leu4460Gln
|
|
XM_011543677.1:c.10763T>A
|
XP_011541979.1:p.Leu3588Gln
|
|
XM_011543678.1:c.13460T>A
|
XP_011541980.1:p.Leu4487Gln
|
|
XM_017009963.2:c.13481T>A
|
XP_016865452.1:p.Leu4494Gln
|
|
XM_017009964.2:c.13478T>A
|
XP_016865453.1:p.Leu4493Gln
|
|
XM_017009965.1:c.13478T>A
|
XP_016865454.1:p.Leu4493Gln
|
|
XM_017009966.2:c.13400T>A
|
XP_016865455.1:p.Leu4467Gln
|
|
XM_017009967.1:c.13385T>A
|
XP_016865456.1:p.Leu4462Gln
|
|
XM_017009968.2:c.13481T>A
|
XP_016865457.1:p.Leu4494Gln
|
|
XM_017009969.2:c.13481T>A
|
XP_016865458.1:p.Leu4494Gln
|
|
XM_017009970.2:c.13481T>A
|
XP_016865459.1:p.Leu4494Gln
|
|
XM_017009971.2:c.13481T>A
|
XP_016865460.1:p.Leu4494Gln
|
|
XM_017009972.1:c.6599T>A
|
XP_016865461.1:p.Leu2200Gln
|
|
XM_017009973.1:c.6578T>A
|
XP_016865462.1:p.Leu2193Gln
|