|
ENST00000375254.8:c.15249A>C
MANE Select
|
ENSP00000364403.3:p.Ala5083=
|
|
|
ENST00000375224.1:c.2370A>C
|
ENSP00000364372.1:p.Ala790=
|
|
|
ENST00000375225.7:c.474A>C
|
ENSP00000364373.3:p.Ala158=
|
|
|
ENST00000375254.7:c.15249A>C
|
ENSP00000364403.3:p.Ala5083=
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|
|
ENST00000459947.5:n.3256A>C
|
|
|
|
NM_020765.2:c.15249A>C
|
NP_065816.2:p.Ala5083=
|
|
|
XM_011541108.1:c.15402A>C
|
XP_011539410.1:p.Ala5134=
|
|
|
XM_011541109.1:c.15399A>C
|
XP_011539411.1:p.Ala5133=
|
|
|
XM_011541110.1:c.15399A>C
|
XP_011539412.1:p.Ala5133=
|
|
|
XM_011541111.1:c.15399A>C
|
XP_011539413.1:p.Ala5133=
|
|
|
XM_011541112.1:c.15387A>C
|
XP_011539414.1:p.Ala5129=
|
|
|
XM_011541113.1:c.15384A>C
|
XP_011539415.1:p.Ala5128=
|
|
|
XM_011541114.1:c.15384A>C
|
XP_011539416.1:p.Ala5128=
|
|
|
XM_011541115.1:c.15378A>C
|
XP_011539417.1:p.Ala5126=
|
|
|
XM_011541116.1:c.15369A>C
|
XP_011539418.1:p.Ala5123=
|
|
|
XM_011541117.1:c.15318A>C
|
XP_011539419.1:p.Ala5106=
|
|
|
XM_011541118.1:c.15315A>C
|
XP_011539420.1:p.Ala5105=
|
|
|
XM_011541119.1:c.15282A>C
|
XP_011539421.1:p.Ala5094=
|
|
|
XM_011541120.1:c.15279A>C
|
XP_011539422.1:p.Ala5093=
|
|
|
XM_011541121.1:c.15246A>C
|
XP_011539423.1:p.Ala5082=
|
|
|
XM_011541108.3:c.15516A>C
|
XP_011539410.2:p.Ala5172=
|
|
|
XM_011541109.3:c.15513A>C
|
XP_011539411.2:p.Ala5171=
|
|
|
XM_011541110.3:c.15513A>C
|
XP_011539412.2:p.Ala5171=
|
|
|
XM_011541111.3:c.15513A>C
|
XP_011539413.2:p.Ala5171=
|
|
|
XM_011541112.3:c.15501A>C
|
XP_011539414.2:p.Ala5167=
|
|
|
XM_011541113.3:c.15498A>C
|
XP_011539415.2:p.Ala5166=
|
|
|
XM_011541114.3:c.15498A>C
|
XP_011539416.2:p.Ala5166=
|
|
|
XM_011541115.3:c.15492A>C
|
XP_011539417.2:p.Ala5164=
|
|
|
XM_011541116.3:c.15483A>C
|
XP_011539418.2:p.Ala5161=
|
|
|
XM_011541117.3:c.15432A>C
|
XP_011539419.2:p.Ala5144=
|
|
|
XM_011541118.3:c.15429A>C
|
XP_011539420.2:p.Ala5143=
|
|
|
XM_011541119.3:c.15396A>C
|
XP_011539421.2:p.Ala5132=
|
|
|
XM_011541120.3:c.15393A>C
|
XP_011539422.2:p.Ala5131=
|
|
|
XM_011541121.3:c.15360A>C
|
XP_011539423.2:p.Ala5120=
|
|
|
XM_017000822.2:c.15495A>C
|
XP_016856311.2:p.Ala5165=
|
|
|
XM_017000823.2:c.15468A>C
|
XP_016856312.2:p.Ala5156=
|
|
|
XM_017000824.2:c.15414A>C
|
XP_016856313.2:p.Ala5138=
|
|
|
XM_017000825.2:c.15399A>C
|
XP_016856314.2:p.Ala5133=
|
|
|
XM_017000826.2:c.15396A>C
|
XP_016856315.2:p.Ala5132=
|
|
|
XM_017000827.2:c.15381A>C
|
XP_016856316.2:p.Ala5127=
|
|
|
XM_017000828.2:c.15357A>C
|
XP_016856317.2:p.Ala5119=
|
|
|
XM_017000829.2:c.15309A>C
|
XP_016856318.2:p.Ala5103=
|
|
|
XM_017000830.2:c.15258A>C
|
XP_016856319.2:p.Ala5086=
|
|
|
NM_020765.3:c.15249A>C
MANE Select
|
NP_065816.2:p.Ala5083=
|
|
