|
ENST00000375254.8:c.15295C>G
MANE Select
|
ENSP00000364403.3:p.Leu5099Val
|
|
|
ENST00000375224.1:c.2416C>G
|
ENSP00000364372.1:p.Leu806Val
|
|
|
ENST00000375225.7:c.520C>G
|
ENSP00000364373.3:p.Leu174Val
|
|
|
ENST00000375254.7:c.15295C>G
|
ENSP00000364403.3:p.Leu5099Val
|
|
|
ENST00000459947.5:n.3302C>G
|
|
|
|
NM_020765.2:c.15295C>G
|
NP_065816.2:p.Leu5099Val
|
|
|
XM_011541108.1:c.15448C>G
|
XP_011539410.1:p.Leu5150Val
|
|
|
XM_011541109.1:c.15445C>G
|
XP_011539411.1:p.Leu5149Val
|
|
|
XM_011541110.1:c.15445C>G
|
XP_011539412.1:p.Leu5149Val
|
|
|
XM_011541111.1:c.15445C>G
|
XP_011539413.1:p.Leu5149Val
|
|
|
XM_011541112.1:c.15433C>G
|
XP_011539414.1:p.Leu5145Val
|
|
|
XM_011541113.1:c.15430C>G
|
XP_011539415.1:p.Leu5144Val
|
|
|
XM_011541114.1:c.15430C>G
|
XP_011539416.1:p.Leu5144Val
|
|
|
XM_011541115.1:c.15424C>G
|
XP_011539417.1:p.Leu5142Val
|
|
|
XM_011541116.1:c.15415C>G
|
XP_011539418.1:p.Leu5139Val
|
|
|
XM_011541117.1:c.15364C>G
|
XP_011539419.1:p.Leu5122Val
|
|
|
XM_011541118.1:c.15361C>G
|
XP_011539420.1:p.Leu5121Val
|
|
|
XM_011541119.1:c.15328C>G
|
XP_011539421.1:p.Leu5110Val
|
|
|
XM_011541120.1:c.15325C>G
|
XP_011539422.1:p.Leu5109Val
|
|
|
XM_011541121.1:c.15292C>G
|
XP_011539423.1:p.Leu5098Val
|
|
|
XM_011541108.3:c.15562C>G
|
XP_011539410.2:p.Leu5188Val
|
|
|
XM_011541109.3:c.15559C>G
|
XP_011539411.2:p.Leu5187Val
|
|
|
XM_011541110.3:c.15559C>G
|
XP_011539412.2:p.Leu5187Val
|
|
|
XM_011541111.3:c.15559C>G
|
XP_011539413.2:p.Leu5187Val
|
|
|
XM_011541112.3:c.15547C>G
|
XP_011539414.2:p.Leu5183Val
|
|
|
XM_011541113.3:c.15544C>G
|
XP_011539415.2:p.Leu5182Val
|
|
|
XM_011541114.3:c.15544C>G
|
XP_011539416.2:p.Leu5182Val
|
|
|
XM_011541115.3:c.15538C>G
|
XP_011539417.2:p.Leu5180Val
|
|
|
XM_011541116.3:c.15529C>G
|
XP_011539418.2:p.Leu5177Val
|
|
|
XM_011541117.3:c.15478C>G
|
XP_011539419.2:p.Leu5160Val
|
|
|
XM_011541118.3:c.15475C>G
|
XP_011539420.2:p.Leu5159Val
|
|
|
XM_011541119.3:c.15442C>G
|
XP_011539421.2:p.Leu5148Val
|
|
|
XM_011541120.3:c.15439C>G
|
XP_011539422.2:p.Leu5147Val
|
|
|
XM_011541121.3:c.15406C>G
|
XP_011539423.2:p.Leu5136Val
|
|
|
XM_017000822.2:c.15541C>G
|
XP_016856311.2:p.Leu5181Val
|
|
|
XM_017000823.2:c.15514C>G
|
XP_016856312.2:p.Leu5172Val
|
|
|
XM_017000824.2:c.15460C>G
|
XP_016856313.2:p.Leu5154Val
|
|
|
XM_017000825.2:c.15445C>G
|
XP_016856314.2:p.Leu5149Val
|
|
|
XM_017000826.2:c.15442C>G
|
XP_016856315.2:p.Leu5148Val
|
|
|
XM_017000827.2:c.15427C>G
|
XP_016856316.2:p.Leu5143Val
|
|
|
XM_017000828.2:c.15403C>G
|
XP_016856317.2:p.Leu5135Val
|
|
|
XM_017000829.2:c.15355C>G
|
XP_016856318.2:p.Leu5119Val
|
|
|
XM_017000830.2:c.15304C>G
|
XP_016856319.2:p.Leu5102Val
|
|
|
NM_020765.3:c.15295C>G
MANE Select
|
NP_065816.2:p.Leu5099Val
|
|
