|
ENST00000375254.8:c.15304C>G
MANE Select
|
ENSP00000364403.3:p.Leu5102Val
|
|
|
ENST00000375224.1:c.2425C>G
|
ENSP00000364372.1:p.Leu809Val
|
|
|
ENST00000375225.7:c.529C>G
|
ENSP00000364373.3:p.Leu177Val
|
|
|
ENST00000375254.7:c.15304C>G
|
ENSP00000364403.3:p.Leu5102Val
|
|
|
ENST00000459947.5:n.3311C>G
|
|
|
|
NM_020765.2:c.15304C>G
|
NP_065816.2:p.Leu5102Val
|
|
|
XM_011541108.1:c.15457C>G
|
XP_011539410.1:p.Leu5153Val
|
|
|
XM_011541109.1:c.15454C>G
|
XP_011539411.1:p.Leu5152Val
|
|
|
XM_011541110.1:c.15454C>G
|
XP_011539412.1:p.Leu5152Val
|
|
|
XM_011541111.1:c.15454C>G
|
XP_011539413.1:p.Leu5152Val
|
|
|
XM_011541112.1:c.15442C>G
|
XP_011539414.1:p.Leu5148Val
|
|
|
XM_011541113.1:c.15439C>G
|
XP_011539415.1:p.Leu5147Val
|
|
|
XM_011541114.1:c.15439C>G
|
XP_011539416.1:p.Leu5147Val
|
|
|
XM_011541115.1:c.15433C>G
|
XP_011539417.1:p.Leu5145Val
|
|
|
XM_011541116.1:c.15424C>G
|
XP_011539418.1:p.Leu5142Val
|
|
|
XM_011541117.1:c.15373C>G
|
XP_011539419.1:p.Leu5125Val
|
|
|
XM_011541118.1:c.15370C>G
|
XP_011539420.1:p.Leu5124Val
|
|
|
XM_011541119.1:c.15337C>G
|
XP_011539421.1:p.Leu5113Val
|
|
|
XM_011541120.1:c.15334C>G
|
XP_011539422.1:p.Leu5112Val
|
|
|
XM_011541121.1:c.15301C>G
|
XP_011539423.1:p.Leu5101Val
|
|
|
XM_011541108.3:c.15571C>G
|
XP_011539410.2:p.Leu5191Val
|
|
|
XM_011541109.3:c.15568C>G
|
XP_011539411.2:p.Leu5190Val
|
|
|
XM_011541110.3:c.15568C>G
|
XP_011539412.2:p.Leu5190Val
|
|
|
XM_011541111.3:c.15568C>G
|
XP_011539413.2:p.Leu5190Val
|
|
|
XM_011541112.3:c.15556C>G
|
XP_011539414.2:p.Leu5186Val
|
|
|
XM_011541113.3:c.15553C>G
|
XP_011539415.2:p.Leu5185Val
|
|
|
XM_011541114.3:c.15553C>G
|
XP_011539416.2:p.Leu5185Val
|
|
|
XM_011541115.3:c.15547C>G
|
XP_011539417.2:p.Leu5183Val
|
|
|
XM_011541116.3:c.15538C>G
|
XP_011539418.2:p.Leu5180Val
|
|
|
XM_011541117.3:c.15487C>G
|
XP_011539419.2:p.Leu5163Val
|
|
|
XM_011541118.3:c.15484C>G
|
XP_011539420.2:p.Leu5162Val
|
|
|
XM_011541119.3:c.15451C>G
|
XP_011539421.2:p.Leu5151Val
|
|
|
XM_011541120.3:c.15448C>G
|
XP_011539422.2:p.Leu5150Val
|
|
|
XM_011541121.3:c.15415C>G
|
XP_011539423.2:p.Leu5139Val
|
|
|
XM_017000822.2:c.15550C>G
|
XP_016856311.2:p.Leu5184Val
|
|
|
XM_017000823.2:c.15523C>G
|
XP_016856312.2:p.Leu5175Val
|
|
|
XM_017000824.2:c.15469C>G
|
XP_016856313.2:p.Leu5157Val
|
|
|
XM_017000825.2:c.15454C>G
|
XP_016856314.2:p.Leu5152Val
|
|
|
XM_017000826.2:c.15451C>G
|
XP_016856315.2:p.Leu5151Val
|
|
|
XM_017000827.2:c.15436C>G
|
XP_016856316.2:p.Leu5146Val
|
|
|
XM_017000828.2:c.15412C>G
|
XP_016856317.2:p.Leu5138Val
|
|
|
XM_017000829.2:c.15364C>G
|
XP_016856318.2:p.Leu5122Val
|
|
|
XM_017000830.2:c.15313C>G
|
XP_016856319.2:p.Leu5105Val
|
|
|
NM_020765.3:c.15304C>G
MANE Select
|
NP_065816.2:p.Leu5102Val
|
|
