|
NM_001369369.1:c.1279C>T
MANE Select
|
NP_001356298.1:p.His427Tyr
|
|
ENST00000579795.6:c.1279C>T
MANE Select
|
ENSP00000464645.1:p.His427Tyr
|
|
NM_003593.2:c.1279C>T , LRG_61t1:c.1279C>T
|
NP_003584.2:p.His427Tyr
|
|
NM_003593.3:c.1279C>T
|
NP_003584.2:p.His427Tyr
|
|
ENST00000226247.2:c.1279C>T
|
ENSP00000226247.2:p.His427Tyr
|
|
ENST00000481916.6:c.*1195+69201G>A
|
ENSP00000436369.2:n.*1195+69201G>A
|
|
ENST00000577936.2:c.1279C>T
|
ENSP00000462159.2:p.His427Tyr
|
|
ENST00000579795.5:c.1279C>T
|
ENSP00000464645.1:p.His427Tyr
|
|
XM_005258046.3:c.1279C>T
|
XP_005258103.1:p.His427Tyr
|
|
XM_011525354.1:c.1336C>T
|
XP_011523656.1:p.His446Tyr
|
|
XM_011525355.1:c.1333C>T
|
XP_011523657.1:p.His445Tyr
|
|
XM_011525356.1:c.1333C>T
|
XP_011523658.1:p.His445Tyr
|
|
XM_011525357.1:c.1315C>T
|
XP_011523659.1:p.His439Tyr
|
|
XM_011525358.1:c.1282C>T
|
XP_011523660.1:p.His428Tyr
|
|
XM_011525359.1:c.1282C>T
|
XP_011523661.1:p.His428Tyr
|
|
XM_011525360.1:c.1282C>T
|
XP_011523662.1:p.His428Tyr
|
|
XM_011525361.1:c.1279C>T
|
XP_011523663.1:p.His427Tyr
|
|
XM_011525362.1:c.1279C>T
|
XP_011523664.1:p.His427Tyr
|
|
XM_011525363.1:c.1193-103C>T
|
XP_011523665.1:n.1193-103C>T
|
|
XM_011525364.1:c.814C>T
|
XP_011523666.1:p.His272Tyr
|
|
XM_011525365.1:c.1192+312C>T
|
XP_011523667.1:n.1192+312C>T
|
|
XM_011525366.1:c.736C>T
|
XP_011523668.1:p.His246Tyr
|
|
XM_011525367.1:c.721C>T
|
XP_011523669.1:p.His241Tyr
|
|
XM_011525368.1:c.643C>T
|
XP_011523670.1:p.His215Tyr
|
|
XM_011525368.2:c.643C>T
|
XP_011523670.1:p.His215Tyr
|
|
XM_011525369.1:c.643C>T
|
XP_011523671.1:p.His215Tyr
|
|
XM_011525369.2:c.643C>T
|
XP_011523671.1:p.His215Tyr
|
|
XM_011525370.1:c.643C>T
|
XP_011523672.1:p.His215Tyr
|
|
XM_011525370.2:c.643C>T
|
XP_011523672.1:p.His215Tyr
|
|
XM_017025228.1:c.1279C>T
|
XP_016880717.1:p.His427Tyr
|
|
XM_017025229.1:c.1139-103C>T
|
XP_016880718.1:n.1139-103C>T
|
|
XM_017025230.1:c.1138+312C>T
|
XP_016880719.1:n.1138+312C>T
|
|
XM_017025231.1:c.1139-144C>T
|
XP_016880720.1:n.1139-144C>T
|
