|
ENST00000375254.8:c.15283C>G
MANE Select
|
ENSP00000364403.3:p.Leu5095Val
|
|
|
ENST00000375224.1:c.2404C>G
|
ENSP00000364372.1:p.Leu802Val
|
|
|
ENST00000375225.7:c.508C>G
|
ENSP00000364373.3:p.Leu170Val
|
|
|
ENST00000375254.7:c.15283C>G
|
ENSP00000364403.3:p.Leu5095Val
|
|
|
ENST00000459947.5:n.3290C>G
|
|
|
|
NM_020765.2:c.15283C>G
|
NP_065816.2:p.Leu5095Val
|
|
|
XM_011541108.1:c.15436C>G
|
XP_011539410.1:p.Leu5146Val
|
|
|
XM_011541109.1:c.15433C>G
|
XP_011539411.1:p.Leu5145Val
|
|
|
XM_011541110.1:c.15433C>G
|
XP_011539412.1:p.Leu5145Val
|
|
|
XM_011541111.1:c.15433C>G
|
XP_011539413.1:p.Leu5145Val
|
|
|
XM_011541112.1:c.15421C>G
|
XP_011539414.1:p.Leu5141Val
|
|
|
XM_011541113.1:c.15418C>G
|
XP_011539415.1:p.Leu5140Val
|
|
|
XM_011541114.1:c.15418C>G
|
XP_011539416.1:p.Leu5140Val
|
|
|
XM_011541115.1:c.15412C>G
|
XP_011539417.1:p.Leu5138Val
|
|
|
XM_011541116.1:c.15403C>G
|
XP_011539418.1:p.Leu5135Val
|
|
|
XM_011541117.1:c.15352C>G
|
XP_011539419.1:p.Leu5118Val
|
|
|
XM_011541118.1:c.15349C>G
|
XP_011539420.1:p.Leu5117Val
|
|
|
XM_011541119.1:c.15316C>G
|
XP_011539421.1:p.Leu5106Val
|
|
|
XM_011541120.1:c.15313C>G
|
XP_011539422.1:p.Leu5105Val
|
|
|
XM_011541121.1:c.15280C>G
|
XP_011539423.1:p.Leu5094Val
|
|
|
XM_011541108.3:c.15550C>G
|
XP_011539410.2:p.Leu5184Val
|
|
|
XM_011541109.3:c.15547C>G
|
XP_011539411.2:p.Leu5183Val
|
|
|
XM_011541110.3:c.15547C>G
|
XP_011539412.2:p.Leu5183Val
|
|
|
XM_011541111.3:c.15547C>G
|
XP_011539413.2:p.Leu5183Val
|
|
|
XM_011541112.3:c.15535C>G
|
XP_011539414.2:p.Leu5179Val
|
|
|
XM_011541113.3:c.15532C>G
|
XP_011539415.2:p.Leu5178Val
|
|
|
XM_011541114.3:c.15532C>G
|
XP_011539416.2:p.Leu5178Val
|
|
|
XM_011541115.3:c.15526C>G
|
XP_011539417.2:p.Leu5176Val
|
|
|
XM_011541116.3:c.15517C>G
|
XP_011539418.2:p.Leu5173Val
|
|
|
XM_011541117.3:c.15466C>G
|
XP_011539419.2:p.Leu5156Val
|
|
|
XM_011541118.3:c.15463C>G
|
XP_011539420.2:p.Leu5155Val
|
|
|
XM_011541119.3:c.15430C>G
|
XP_011539421.2:p.Leu5144Val
|
|
|
XM_011541120.3:c.15427C>G
|
XP_011539422.2:p.Leu5143Val
|
|
|
XM_011541121.3:c.15394C>G
|
XP_011539423.2:p.Leu5132Val
|
|
|
XM_017000822.2:c.15529C>G
|
XP_016856311.2:p.Leu5177Val
|
|
|
XM_017000823.2:c.15502C>G
|
XP_016856312.2:p.Leu5168Val
|
|
|
XM_017000824.2:c.15448C>G
|
XP_016856313.2:p.Leu5150Val
|
|
|
XM_017000825.2:c.15433C>G
|
XP_016856314.2:p.Leu5145Val
|
|
|
XM_017000826.2:c.15430C>G
|
XP_016856315.2:p.Leu5144Val
|
|
|
XM_017000827.2:c.15415C>G
|
XP_016856316.2:p.Leu5139Val
|
|
|
XM_017000828.2:c.15391C>G
|
XP_016856317.2:p.Leu5131Val
|
|
|
XM_017000829.2:c.15343C>G
|
XP_016856318.2:p.Leu5115Val
|
|
|
XM_017000830.2:c.15292C>G
|
XP_016856319.2:p.Leu5098Val
|
|
|
NM_020765.3:c.15283C>G
MANE Select
|
NP_065816.2:p.Leu5095Val
|
|
