|
ENST00000375254.8:c.15321T>C
MANE Select
|
ENSP00000364403.3:p.Phe5107=
|
|
|
ENST00000375224.1:c.2442T>C
|
ENSP00000364372.1:p.Phe814=
|
|
|
ENST00000375225.7:c.546T>C
|
ENSP00000364373.3:p.Phe182=
|
|
|
ENST00000375254.7:c.15321T>C
|
ENSP00000364403.3:p.Phe5107=
|
|
|
ENST00000459947.5:n.3328T>C
|
|
|
|
NM_020765.2:c.15321T>C
|
NP_065816.2:p.Phe5107=
|
|
|
XM_011541108.1:c.15474T>C
|
XP_011539410.1:p.Phe5158=
|
|
|
XM_011541109.1:c.15471T>C
|
XP_011539411.1:p.Phe5157=
|
|
|
XM_011541110.1:c.15471T>C
|
XP_011539412.1:p.Phe5157=
|
|
|
XM_011541111.1:c.15471T>C
|
XP_011539413.1:p.Phe5157=
|
|
|
XM_011541112.1:c.15459T>C
|
XP_011539414.1:p.Phe5153=
|
|
|
XM_011541113.1:c.15456T>C
|
XP_011539415.1:p.Phe5152=
|
|
|
XM_011541114.1:c.15456T>C
|
XP_011539416.1:p.Phe5152=
|
|
|
XM_011541115.1:c.15450T>C
|
XP_011539417.1:p.Phe5150=
|
|
|
XM_011541116.1:c.15441T>C
|
XP_011539418.1:p.Phe5147=
|
|
|
XM_011541117.1:c.15390T>C
|
XP_011539419.1:p.Phe5130=
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|
|
XM_011541118.1:c.15387T>C
|
XP_011539420.1:p.Phe5129=
|
|
|
XM_011541119.1:c.15354T>C
|
XP_011539421.1:p.Phe5118=
|
|
|
XM_011541120.1:c.15351T>C
|
XP_011539422.1:p.Phe5117=
|
|
|
XM_011541121.1:c.15318T>C
|
XP_011539423.1:p.Phe5106=
|
|
|
XM_011541108.3:c.15588T>C
|
XP_011539410.2:p.Phe5196=
|
|
|
XM_011541109.3:c.15585T>C
|
XP_011539411.2:p.Phe5195=
|
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XM_011541110.3:c.15585T>C
|
XP_011539412.2:p.Phe5195=
|
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|
XM_011541111.3:c.15585T>C
|
XP_011539413.2:p.Phe5195=
|
|
|
XM_011541112.3:c.15573T>C
|
XP_011539414.2:p.Phe5191=
|
|
|
XM_011541113.3:c.15570T>C
|
XP_011539415.2:p.Phe5190=
|
|
|
XM_011541114.3:c.15570T>C
|
XP_011539416.2:p.Phe5190=
|
|
|
XM_011541115.3:c.15564T>C
|
XP_011539417.2:p.Phe5188=
|
|
|
XM_011541116.3:c.15555T>C
|
XP_011539418.2:p.Phe5185=
|
|
|
XM_011541117.3:c.15504T>C
|
XP_011539419.2:p.Phe5168=
|
|
|
XM_011541118.3:c.15501T>C
|
XP_011539420.2:p.Phe5167=
|
|
|
XM_011541119.3:c.15468T>C
|
XP_011539421.2:p.Phe5156=
|
|
|
XM_011541120.3:c.15465T>C
|
XP_011539422.2:p.Phe5155=
|
|
|
XM_011541121.3:c.15432T>C
|
XP_011539423.2:p.Phe5144=
|
|
|
XM_017000822.2:c.15567T>C
|
XP_016856311.2:p.Phe5189=
|
|
|
XM_017000823.2:c.15540T>C
|
XP_016856312.2:p.Phe5180=
|
|
|
XM_017000824.2:c.15486T>C
|
XP_016856313.2:p.Phe5162=
|
|
|
XM_017000825.2:c.15471T>C
|
XP_016856314.2:p.Phe5157=
|
|
|
XM_017000826.2:c.15468T>C
|
XP_016856315.2:p.Phe5156=
|
|
|
XM_017000827.2:c.15453T>C
|
XP_016856316.2:p.Phe5151=
|
|
|
XM_017000828.2:c.15429T>C
|
XP_016856317.2:p.Phe5143=
|
|
|
XM_017000829.2:c.15381T>C
|
XP_016856318.2:p.Phe5127=
|
|
|
XM_017000830.2:c.15330T>C
|
XP_016856319.2:p.Phe5110=
|
|
|
NM_020765.3:c.15321T>C
MANE Select
|
NP_065816.2:p.Phe5107=
|
|
