|
ENST00000375254.8:c.15286T>G
MANE Select
|
ENSP00000364403.3:p.Phe5096Val
|
|
|
ENST00000375224.1:c.2407T>G
|
ENSP00000364372.1:p.Phe803Val
|
|
|
ENST00000375225.7:c.511T>G
|
ENSP00000364373.3:p.Phe171Val
|
|
|
ENST00000375254.7:c.15286T>G
|
ENSP00000364403.3:p.Phe5096Val
|
|
|
ENST00000459947.5:n.3293T>G
|
|
|
|
NM_020765.2:c.15286T>G
|
NP_065816.2:p.Phe5096Val
|
|
|
XM_011541108.1:c.15439T>G
|
XP_011539410.1:p.Phe5147Val
|
|
|
XM_011541109.1:c.15436T>G
|
XP_011539411.1:p.Phe5146Val
|
|
|
XM_011541110.1:c.15436T>G
|
XP_011539412.1:p.Phe5146Val
|
|
|
XM_011541111.1:c.15436T>G
|
XP_011539413.1:p.Phe5146Val
|
|
|
XM_011541112.1:c.15424T>G
|
XP_011539414.1:p.Phe5142Val
|
|
|
XM_011541113.1:c.15421T>G
|
XP_011539415.1:p.Phe5141Val
|
|
|
XM_011541114.1:c.15421T>G
|
XP_011539416.1:p.Phe5141Val
|
|
|
XM_011541115.1:c.15415T>G
|
XP_011539417.1:p.Phe5139Val
|
|
|
XM_011541116.1:c.15406T>G
|
XP_011539418.1:p.Phe5136Val
|
|
|
XM_011541117.1:c.15355T>G
|
XP_011539419.1:p.Phe5119Val
|
|
|
XM_011541118.1:c.15352T>G
|
XP_011539420.1:p.Phe5118Val
|
|
|
XM_011541119.1:c.15319T>G
|
XP_011539421.1:p.Phe5107Val
|
|
|
XM_011541120.1:c.15316T>G
|
XP_011539422.1:p.Phe5106Val
|
|
|
XM_011541121.1:c.15283T>G
|
XP_011539423.1:p.Phe5095Val
|
|
|
XM_011541108.3:c.15553T>G
|
XP_011539410.2:p.Phe5185Val
|
|
|
XM_011541109.3:c.15550T>G
|
XP_011539411.2:p.Phe5184Val
|
|
|
XM_011541110.3:c.15550T>G
|
XP_011539412.2:p.Phe5184Val
|
|
|
XM_011541111.3:c.15550T>G
|
XP_011539413.2:p.Phe5184Val
|
|
|
XM_011541112.3:c.15538T>G
|
XP_011539414.2:p.Phe5180Val
|
|
|
XM_011541113.3:c.15535T>G
|
XP_011539415.2:p.Phe5179Val
|
|
|
XM_011541114.3:c.15535T>G
|
XP_011539416.2:p.Phe5179Val
|
|
|
XM_011541115.3:c.15529T>G
|
XP_011539417.2:p.Phe5177Val
|
|
|
XM_011541116.3:c.15520T>G
|
XP_011539418.2:p.Phe5174Val
|
|
|
XM_011541117.3:c.15469T>G
|
XP_011539419.2:p.Phe5157Val
|
|
|
XM_011541118.3:c.15466T>G
|
XP_011539420.2:p.Phe5156Val
|
|
|
XM_011541119.3:c.15433T>G
|
XP_011539421.2:p.Phe5145Val
|
|
|
XM_011541120.3:c.15430T>G
|
XP_011539422.2:p.Phe5144Val
|
|
|
XM_011541121.3:c.15397T>G
|
XP_011539423.2:p.Phe5133Val
|
|
|
XM_017000822.2:c.15532T>G
|
XP_016856311.2:p.Phe5178Val
|
|
|
XM_017000823.2:c.15505T>G
|
XP_016856312.2:p.Phe5169Val
|
|
|
XM_017000824.2:c.15451T>G
|
XP_016856313.2:p.Phe5151Val
|
|
|
XM_017000825.2:c.15436T>G
|
XP_016856314.2:p.Phe5146Val
|
|
|
XM_017000826.2:c.15433T>G
|
XP_016856315.2:p.Phe5145Val
|
|
|
XM_017000827.2:c.15418T>G
|
XP_016856316.2:p.Phe5140Val
|
|
|
XM_017000828.2:c.15394T>G
|
XP_016856317.2:p.Phe5132Val
|
|
|
XM_017000829.2:c.15346T>G
|
XP_016856318.2:p.Phe5116Val
|
|
|
XM_017000830.2:c.15295T>G
|
XP_016856319.2:p.Phe5099Val
|
|
|
NM_020765.3:c.15286T>G
MANE Select
|
NP_065816.2:p.Phe5096Val
|
|
