ENST00000461280.2:n.1499G>A
|
|
|
ENST00000684241.1:n.3034G>A
|
|
|
ENST00000262186.10:c.2201G>A
MANE Select
|
ENSP00000262186.5:p.Arg734His
|
|
ENST00000330883.9:c.1181G>A
|
ENSP00000328531.4:p.Arg394His
|
|
ENST00000262186.9:c.2201G>A
|
ENSP00000262186.5:p.Arg734His
|
|
ENST00000330883.8:c.1181G>A
|
ENSP00000328531.4:p.Arg394His
|
|
ENST00000430723.4:c.1853G>A
|
ENSP00000387657.4:p.Arg618His
|
|
ENST00000461280.1:n.1488G>A
|
|
|
ENST00000473610.5:n.1833G>A
|
|
|
ENST00000532957.5:n.2424G>A
|
|
|
NM_000238.3:c.2201G>A , LRG_288t1:c.2201G>A
|
NP_000229.1:p.Arg734His
|
|
NM_001204798.1:c.1181G>A
|
NP_001191727.1:p.Arg394His
|
|
NM_172056.2:c.2201G>A , LRG_288t2:c.2201G>A
|
NP_742053.1:p.Arg734His
|
|
NM_172057.2:c.1181G>A , LRG_288t3:c.1181G>A
|
NP_742054.1:p.Arg394His
|
|
XM_011516185.1:c.1901G>A
|
XP_011514487.1:p.Arg634His
|
|
XM_011516186.1:c.2201G>A
|
XP_011514488.1:p.Arg734His
|
|
XM_011516185.2:c.1901G>A
|
XP_011514487.1:p.Arg634His
|
|
XM_011516186.3:c.2201G>A
|
XP_011514488.1:p.Arg734His
|
|
XM_017012195.1:c.2051G>A
|
XP_016867684.1:p.Arg684His
|
|
XM_017012196.1:c.2024G>A
|
XP_016867685.1:p.Arg675His
|
|
NM_000238.4:c.2201G>A
MANE Select
|
NP_000229.1:p.Arg734His
|
|
NM_001204798.2:c.1181G>A
|
NP_001191727.1:p.Arg394His
|
|
NM_172057.3:c.1181G>A
|
NP_742054.1:p.Arg394His
|
|