|
ENST00000375254.8:c.15319T>G
MANE Select
|
ENSP00000364403.3:p.Phe5107Val
|
|
|
ENST00000375224.1:c.2440T>G
|
ENSP00000364372.1:p.Phe814Val
|
|
|
ENST00000375225.7:c.544T>G
|
ENSP00000364373.3:p.Phe182Val
|
|
|
ENST00000375254.7:c.15319T>G
|
ENSP00000364403.3:p.Phe5107Val
|
|
|
ENST00000459947.5:n.3326T>G
|
|
|
|
NM_020765.2:c.15319T>G
|
NP_065816.2:p.Phe5107Val
|
|
|
XM_011541108.1:c.15472T>G
|
XP_011539410.1:p.Phe5158Val
|
|
|
XM_011541109.1:c.15469T>G
|
XP_011539411.1:p.Phe5157Val
|
|
|
XM_011541110.1:c.15469T>G
|
XP_011539412.1:p.Phe5157Val
|
|
|
XM_011541111.1:c.15469T>G
|
XP_011539413.1:p.Phe5157Val
|
|
|
XM_011541112.1:c.15457T>G
|
XP_011539414.1:p.Phe5153Val
|
|
|
XM_011541113.1:c.15454T>G
|
XP_011539415.1:p.Phe5152Val
|
|
|
XM_011541114.1:c.15454T>G
|
XP_011539416.1:p.Phe5152Val
|
|
|
XM_011541115.1:c.15448T>G
|
XP_011539417.1:p.Phe5150Val
|
|
|
XM_011541116.1:c.15439T>G
|
XP_011539418.1:p.Phe5147Val
|
|
|
XM_011541117.1:c.15388T>G
|
XP_011539419.1:p.Phe5130Val
|
|
|
XM_011541118.1:c.15385T>G
|
XP_011539420.1:p.Phe5129Val
|
|
|
XM_011541119.1:c.15352T>G
|
XP_011539421.1:p.Phe5118Val
|
|
|
XM_011541120.1:c.15349T>G
|
XP_011539422.1:p.Phe5117Val
|
|
|
XM_011541121.1:c.15316T>G
|
XP_011539423.1:p.Phe5106Val
|
|
|
XM_011541108.3:c.15586T>G
|
XP_011539410.2:p.Phe5196Val
|
|
|
XM_011541109.3:c.15583T>G
|
XP_011539411.2:p.Phe5195Val
|
|
|
XM_011541110.3:c.15583T>G
|
XP_011539412.2:p.Phe5195Val
|
|
|
XM_011541111.3:c.15583T>G
|
XP_011539413.2:p.Phe5195Val
|
|
|
XM_011541112.3:c.15571T>G
|
XP_011539414.2:p.Phe5191Val
|
|
|
XM_011541113.3:c.15568T>G
|
XP_011539415.2:p.Phe5190Val
|
|
|
XM_011541114.3:c.15568T>G
|
XP_011539416.2:p.Phe5190Val
|
|
|
XM_011541115.3:c.15562T>G
|
XP_011539417.2:p.Phe5188Val
|
|
|
XM_011541116.3:c.15553T>G
|
XP_011539418.2:p.Phe5185Val
|
|
|
XM_011541117.3:c.15502T>G
|
XP_011539419.2:p.Phe5168Val
|
|
|
XM_011541118.3:c.15499T>G
|
XP_011539420.2:p.Phe5167Val
|
|
|
XM_011541119.3:c.15466T>G
|
XP_011539421.2:p.Phe5156Val
|
|
|
XM_011541120.3:c.15463T>G
|
XP_011539422.2:p.Phe5155Val
|
|
|
XM_011541121.3:c.15430T>G
|
XP_011539423.2:p.Phe5144Val
|
|
|
XM_017000822.2:c.15565T>G
|
XP_016856311.2:p.Phe5189Val
|
|
|
XM_017000823.2:c.15538T>G
|
XP_016856312.2:p.Phe5180Val
|
|
|
XM_017000824.2:c.15484T>G
|
XP_016856313.2:p.Phe5162Val
|
|
|
XM_017000825.2:c.15469T>G
|
XP_016856314.2:p.Phe5157Val
|
|
|
XM_017000826.2:c.15466T>G
|
XP_016856315.2:p.Phe5156Val
|
|
|
XM_017000827.2:c.15451T>G
|
XP_016856316.2:p.Phe5151Val
|
|
|
XM_017000828.2:c.15427T>G
|
XP_016856317.2:p.Phe5143Val
|
|
|
XM_017000829.2:c.15379T>G
|
XP_016856318.2:p.Phe5127Val
|
|
|
XM_017000830.2:c.15328T>G
|
XP_016856319.2:p.Phe5110Val
|
|
|
NM_020765.3:c.15319T>G
MANE Select
|
NP_065816.2:p.Phe5107Val
|
|
