|
ENST00000375254.8:c.15237G>C
MANE Select
|
ENSP00000364403.3:p.Leu5079=
|
|
|
ENST00000375224.1:c.2358G>C
|
ENSP00000364372.1:p.Leu786=
|
|
|
ENST00000375225.7:c.462G>C
|
ENSP00000364373.3:p.Leu154=
|
|
|
ENST00000375254.7:c.15237G>C
|
ENSP00000364403.3:p.Leu5079=
|
|
|
ENST00000459947.5:n.3244G>C
|
|
|
|
NM_020765.2:c.15237G>C
|
NP_065816.2:p.Leu5079=
|
|
|
XM_011541108.1:c.15390G>C
|
XP_011539410.1:p.Leu5130=
|
|
|
XM_011541109.1:c.15387G>C
|
XP_011539411.1:p.Leu5129=
|
|
|
XM_011541110.1:c.15387G>C
|
XP_011539412.1:p.Leu5129=
|
|
|
XM_011541111.1:c.15387G>C
|
XP_011539413.1:p.Leu5129=
|
|
|
XM_011541112.1:c.15375G>C
|
XP_011539414.1:p.Leu5125=
|
|
|
XM_011541113.1:c.15372G>C
|
XP_011539415.1:p.Leu5124=
|
|
|
XM_011541114.1:c.15372G>C
|
XP_011539416.1:p.Leu5124=
|
|
|
XM_011541115.1:c.15366G>C
|
XP_011539417.1:p.Leu5122=
|
|
|
XM_011541116.1:c.15357G>C
|
XP_011539418.1:p.Leu5119=
|
|
|
XM_011541117.1:c.15306G>C
|
XP_011539419.1:p.Leu5102=
|
|
|
XM_011541118.1:c.15303G>C
|
XP_011539420.1:p.Leu5101=
|
|
|
XM_011541119.1:c.15270G>C
|
XP_011539421.1:p.Leu5090=
|
|
|
XM_011541120.1:c.15267G>C
|
XP_011539422.1:p.Leu5089=
|
|
|
XM_011541121.1:c.15234G>C
|
XP_011539423.1:p.Leu5078=
|
|
|
XM_011541108.3:c.15504G>C
|
XP_011539410.2:p.Leu5168=
|
|
|
XM_011541109.3:c.15501G>C
|
XP_011539411.2:p.Leu5167=
|
|
|
XM_011541110.3:c.15501G>C
|
XP_011539412.2:p.Leu5167=
|
|
|
XM_011541111.3:c.15501G>C
|
XP_011539413.2:p.Leu5167=
|
|
|
XM_011541112.3:c.15489G>C
|
XP_011539414.2:p.Leu5163=
|
|
|
XM_011541113.3:c.15486G>C
|
XP_011539415.2:p.Leu5162=
|
|
|
XM_011541114.3:c.15486G>C
|
XP_011539416.2:p.Leu5162=
|
|
|
XM_011541115.3:c.15480G>C
|
XP_011539417.2:p.Leu5160=
|
|
|
XM_011541116.3:c.15471G>C
|
XP_011539418.2:p.Leu5157=
|
|
|
XM_011541117.3:c.15420G>C
|
XP_011539419.2:p.Leu5140=
|
|
|
XM_011541118.3:c.15417G>C
|
XP_011539420.2:p.Leu5139=
|
|
|
XM_011541119.3:c.15384G>C
|
XP_011539421.2:p.Leu5128=
|
|
|
XM_011541120.3:c.15381G>C
|
XP_011539422.2:p.Leu5127=
|
|
|
XM_011541121.3:c.15348G>C
|
XP_011539423.2:p.Leu5116=
|
|
|
XM_017000822.2:c.15483G>C
|
XP_016856311.2:p.Leu5161=
|
|
|
XM_017000823.2:c.15456G>C
|
XP_016856312.2:p.Leu5152=
|
|
|
XM_017000824.2:c.15402G>C
|
XP_016856313.2:p.Leu5134=
|
|
|
XM_017000825.2:c.15387G>C
|
XP_016856314.2:p.Leu5129=
|
|
|
XM_017000826.2:c.15384G>C
|
XP_016856315.2:p.Leu5128=
|
|
|
XM_017000827.2:c.15369G>C
|
XP_016856316.2:p.Leu5123=
|
|
|
XM_017000828.2:c.15345G>C
|
XP_016856317.2:p.Leu5115=
|
|
|
XM_017000829.2:c.15297G>C
|
XP_016856318.2:p.Leu5099=
|
|
|
XM_017000830.2:c.15246G>C
|
XP_016856319.2:p.Leu5082=
|
|
|
NM_020765.3:c.15237G>C
MANE Select
|
NP_065816.2:p.Leu5079=
|
|
