|
ENST00000375254.8:c.15299T>G
MANE Select
|
ENSP00000364403.3:p.Val5100Gly
|
|
|
ENST00000375224.1:c.2420T>G
|
ENSP00000364372.1:p.Val807Gly
|
|
|
ENST00000375225.7:c.524T>G
|
ENSP00000364373.3:p.Val175Gly
|
|
|
ENST00000375254.7:c.15299T>G
|
ENSP00000364403.3:p.Val5100Gly
|
|
|
ENST00000459947.5:n.3306T>G
|
|
|
|
NM_020765.2:c.15299T>G
|
NP_065816.2:p.Val5100Gly
|
|
|
XM_011541108.1:c.15452T>G
|
XP_011539410.1:p.Val5151Gly
|
|
|
XM_011541109.1:c.15449T>G
|
XP_011539411.1:p.Val5150Gly
|
|
|
XM_011541110.1:c.15449T>G
|
XP_011539412.1:p.Val5150Gly
|
|
|
XM_011541111.1:c.15449T>G
|
XP_011539413.1:p.Val5150Gly
|
|
|
XM_011541112.1:c.15437T>G
|
XP_011539414.1:p.Val5146Gly
|
|
|
XM_011541113.1:c.15434T>G
|
XP_011539415.1:p.Val5145Gly
|
|
|
XM_011541114.1:c.15434T>G
|
XP_011539416.1:p.Val5145Gly
|
|
|
XM_011541115.1:c.15428T>G
|
XP_011539417.1:p.Val5143Gly
|
|
|
XM_011541116.1:c.15419T>G
|
XP_011539418.1:p.Val5140Gly
|
|
|
XM_011541117.1:c.15368T>G
|
XP_011539419.1:p.Val5123Gly
|
|
|
XM_011541118.1:c.15365T>G
|
XP_011539420.1:p.Val5122Gly
|
|
|
XM_011541119.1:c.15332T>G
|
XP_011539421.1:p.Val5111Gly
|
|
|
XM_011541120.1:c.15329T>G
|
XP_011539422.1:p.Val5110Gly
|
|
|
XM_011541121.1:c.15296T>G
|
XP_011539423.1:p.Val5099Gly
|
|
|
XM_011541108.3:c.15566T>G
|
XP_011539410.2:p.Val5189Gly
|
|
|
XM_011541109.3:c.15563T>G
|
XP_011539411.2:p.Val5188Gly
|
|
|
XM_011541110.3:c.15563T>G
|
XP_011539412.2:p.Val5188Gly
|
|
|
XM_011541111.3:c.15563T>G
|
XP_011539413.2:p.Val5188Gly
|
|
|
XM_011541112.3:c.15551T>G
|
XP_011539414.2:p.Val5184Gly
|
|
|
XM_011541113.3:c.15548T>G
|
XP_011539415.2:p.Val5183Gly
|
|
|
XM_011541114.3:c.15548T>G
|
XP_011539416.2:p.Val5183Gly
|
|
|
XM_011541115.3:c.15542T>G
|
XP_011539417.2:p.Val5181Gly
|
|
|
XM_011541116.3:c.15533T>G
|
XP_011539418.2:p.Val5178Gly
|
|
|
XM_011541117.3:c.15482T>G
|
XP_011539419.2:p.Val5161Gly
|
|
|
XM_011541118.3:c.15479T>G
|
XP_011539420.2:p.Val5160Gly
|
|
|
XM_011541119.3:c.15446T>G
|
XP_011539421.2:p.Val5149Gly
|
|
|
XM_011541120.3:c.15443T>G
|
XP_011539422.2:p.Val5148Gly
|
|
|
XM_011541121.3:c.15410T>G
|
XP_011539423.2:p.Val5137Gly
|
|
|
XM_017000822.2:c.15545T>G
|
XP_016856311.2:p.Val5182Gly
|
|
|
XM_017000823.2:c.15518T>G
|
XP_016856312.2:p.Val5173Gly
|
|
|
XM_017000824.2:c.15464T>G
|
XP_016856313.2:p.Val5155Gly
|
|
|
XM_017000825.2:c.15449T>G
|
XP_016856314.2:p.Val5150Gly
|
|
|
XM_017000826.2:c.15446T>G
|
XP_016856315.2:p.Val5149Gly
|
|
|
XM_017000827.2:c.15431T>G
|
XP_016856316.2:p.Val5144Gly
|
|
|
XM_017000828.2:c.15407T>G
|
XP_016856317.2:p.Val5136Gly
|
|
|
XM_017000829.2:c.15359T>G
|
XP_016856318.2:p.Val5120Gly
|
|
|
XM_017000830.2:c.15308T>G
|
XP_016856319.2:p.Val5103Gly
|
|
|
NM_020765.3:c.15299T>G
MANE Select
|
NP_065816.2:p.Val5100Gly
|
|
