|
ENST00000460011.6:c.-95C>G
|
ENSP00000507070.1:n.-95C>G
|
|
|
ENST00000494498.2:c.104C>G
|
ENSP00000507847.1:p.Thr35Arg
|
|
|
ENST00000397746.8:c.1370C>G
MANE Select
|
ENSP00000380854.3:p.Thr457Arg
|
|
|
ENST00000291670.9:c.1370C>G
|
ENSP00000291670.5:p.Thr457Arg
|
|
|
ENST00000397743.1:c.1326C>G
|
ENSP00000380851.1:p.Asp442Glu
|
|
|
ENST00000397746.7:c.1370C>G
|
ENSP00000380854.3:p.Thr457Arg
|
|
|
ENST00000397748.5:c.1370C>G
|
ENSP00000380856.1:p.Thr457Arg
|
|
|
ENST00000460011.5:n.699C>G
|
|
|
|
ENST00000488577.1:n.396C>G
|
|
|
|
ENST00000494498.1:n.671C>G
|
|
|
|
ENST00000498355.6:n.1439C>G
|
|
|
|
NM_006657.2:c.1370C>G
|
NP_006648.1:p.Thr457Arg
|
|
|
NM_206965.1:c.1370C>G
|
NP_996848.1:p.Thr457Arg
|
|
|
XM_006723961.2:c.1619C>G
|
XP_006724024.2:p.Thr540Arg
|
|
|
XM_006723962.2:c.1619C>G
|
XP_006724025.2:p.Thr540Arg
|
|
|
XM_011529434.1:c.1619C>G
|
XP_011527736.1:p.Thr540Arg
|
|
|
XM_011529435.1:c.1490C>G
|
XP_011527737.1:p.Thr497Arg
|
|
|
XM_011529436.1:c.1619C>G
|
XP_011527738.1:p.Thr540Arg
|
|
|
XM_011529437.1:c.1619C>G
|
XP_011527739.1:p.Thr540Arg
|
|
|
XM_011529438.1:c.1490C>G
|
XP_011527740.1:p.Thr497Arg
|
|
|
XM_011529439.1:c.1106C>G
|
XP_011527741.1:p.Thr369Arg
|
|
|
XR_937433.1:n.1802C>G
|
|
|
|
NM_001320412.1:c.1370C>G
|
NP_001307341.1:p.Thr457Arg
|
|
|
XM_006723961.4:c.1619C>G
|
XP_006724024.2:p.Thr540Arg
|
|
|
XM_006723962.4:c.1619C>G
|
XP_006724025.2:p.Thr540Arg
|
|
|
XM_011529434.3:c.1619C>G
|
XP_011527736.1:p.Thr540Arg
|
|
|
XM_011529435.3:c.1490C>G
|
XP_011527737.1:p.Thr497Arg
|
|
|
XM_011529436.3:c.1619C>G
|
XP_011527738.1:p.Thr540Arg
|
|
|
XM_011529437.3:c.1619C>G
|
XP_011527739.1:p.Thr540Arg
|
|
|
XM_011529439.2:c.1106C>G
|
XP_011527741.1:p.Thr369Arg
|
|
|
XR_937433.3:n.1836C>G
|
|
|
|
NM_206965.2:c.1370C>G
MANE Select
|
NP_996848.1:p.Thr457Arg
|
|
|
NM_001320412.2:c.1370C>G
|
NP_001307341.1:p.Thr457Arg
|
|
|
NM_006657.3:c.1370C>G
|
NP_006648.1:p.Thr457Arg
|
|
