ENST00000375254.8:c.15312C>G
MANE Select
|
ENSP00000364403.3:p.Tyr5104Ter
|
|
ENST00000375224.1:c.2433C>G
|
ENSP00000364372.1:p.Tyr811Ter
|
|
ENST00000375225.7:c.537C>G
|
ENSP00000364373.3:p.Tyr179Ter
|
|
ENST00000375254.7:c.15312C>G
|
ENSP00000364403.3:p.Tyr5104Ter
|
|
ENST00000459947.5:n.3319C>G
|
|
|
NM_020765.2:c.15312C>G
|
NP_065816.2:p.Tyr5104Ter
|
|
XM_011541108.1:c.15465C>G
|
XP_011539410.1:p.Tyr5155Ter
|
|
XM_011541109.1:c.15462C>G
|
XP_011539411.1:p.Tyr5154Ter
|
|
XM_011541110.1:c.15462C>G
|
XP_011539412.1:p.Tyr5154Ter
|
|
XM_011541111.1:c.15462C>G
|
XP_011539413.1:p.Tyr5154Ter
|
|
XM_011541112.1:c.15450C>G
|
XP_011539414.1:p.Tyr5150Ter
|
|
XM_011541113.1:c.15447C>G
|
XP_011539415.1:p.Tyr5149Ter
|
|
XM_011541114.1:c.15447C>G
|
XP_011539416.1:p.Tyr5149Ter
|
|
XM_011541115.1:c.15441C>G
|
XP_011539417.1:p.Tyr5147Ter
|
|
XM_011541116.1:c.15432C>G
|
XP_011539418.1:p.Tyr5144Ter
|
|
XM_011541117.1:c.15381C>G
|
XP_011539419.1:p.Tyr5127Ter
|
|
XM_011541118.1:c.15378C>G
|
XP_011539420.1:p.Tyr5126Ter
|
|
XM_011541119.1:c.15345C>G
|
XP_011539421.1:p.Tyr5115Ter
|
|
XM_011541120.1:c.15342C>G
|
XP_011539422.1:p.Tyr5114Ter
|
|
XM_011541121.1:c.15309C>G
|
XP_011539423.1:p.Tyr5103Ter
|
|
XM_011541108.3:c.15579C>G
|
XP_011539410.2:p.Tyr5193Ter
|
|
XM_011541109.3:c.15576C>G
|
XP_011539411.2:p.Tyr5192Ter
|
|
XM_011541110.3:c.15576C>G
|
XP_011539412.2:p.Tyr5192Ter
|
|
XM_011541111.3:c.15576C>G
|
XP_011539413.2:p.Tyr5192Ter
|
|
XM_011541112.3:c.15564C>G
|
XP_011539414.2:p.Tyr5188Ter
|
|
XM_011541113.3:c.15561C>G
|
XP_011539415.2:p.Tyr5187Ter
|
|
XM_011541114.3:c.15561C>G
|
XP_011539416.2:p.Tyr5187Ter
|
|
XM_011541115.3:c.15555C>G
|
XP_011539417.2:p.Tyr5185Ter
|
|
XM_011541116.3:c.15546C>G
|
XP_011539418.2:p.Tyr5182Ter
|
|
XM_011541117.3:c.15495C>G
|
XP_011539419.2:p.Tyr5165Ter
|
|
XM_011541118.3:c.15492C>G
|
XP_011539420.2:p.Tyr5164Ter
|
|
XM_011541119.3:c.15459C>G
|
XP_011539421.2:p.Tyr5153Ter
|
|
XM_011541120.3:c.15456C>G
|
XP_011539422.2:p.Tyr5152Ter
|
|
XM_011541121.3:c.15423C>G
|
XP_011539423.2:p.Tyr5141Ter
|
|
XM_017000822.2:c.15558C>G
|
XP_016856311.2:p.Tyr5186Ter
|
|
XM_017000823.2:c.15531C>G
|
XP_016856312.2:p.Tyr5177Ter
|
|
XM_017000824.2:c.15477C>G
|
XP_016856313.2:p.Tyr5159Ter
|
|
XM_017000825.2:c.15462C>G
|
XP_016856314.2:p.Tyr5154Ter
|
|
XM_017000826.2:c.15459C>G
|
XP_016856315.2:p.Tyr5153Ter
|
|
XM_017000827.2:c.15444C>G
|
XP_016856316.2:p.Tyr5148Ter
|
|
XM_017000828.2:c.15420C>G
|
XP_016856317.2:p.Tyr5140Ter
|
|
XM_017000829.2:c.15372C>G
|
XP_016856318.2:p.Tyr5124Ter
|
|
XM_017000830.2:c.15321C>G
|
XP_016856319.2:p.Tyr5107Ter
|
|
NM_020765.3:c.15312C>G
MANE Select
|
NP_065816.2:p.Tyr5104Ter
|
|