|
ENST00000233202.11:c.151G>C
MANE Select
|
ENSP00000233202.6:p.Gly51Arg
|
|
|
ENST00000233202.10:c.151G>C
|
ENSP00000233202.6:p.Gly51Arg
|
|
|
ENST00000354352.9:c.151G>C
|
ENSP00000346320.5:p.Gly51Arg
|
|
|
ENST00000465984.5:n.332-904G>C
|
|
|
|
ENST00000468221.5:n.1631G>C
|
|
|
|
ENST00000469449.1:n.557G>C
|
|
|
|
ENST00000469799.5:n.98-904G>C
|
|
|
|
ENST00000471875.5:n.98G>C
|
|
|
|
ENST00000473367.5:c.151-76G>C
|
ENSP00000484905.1:n.151-76G>C
|
|
|
ENST00000475225.5:n.186-76G>C
|
|
|
|
ENST00000481524.5:c.8-904G>C
|
ENSP00000483970.1:n.8-904G>C
|
|
|
ENST00000483487.2:n.77G>C
|
|
|
|
ENST00000492413.5:n.233G>C
|
|
|
|
ENST00000494322.5:n.247G>C
|
|
|
|
ENST00000539932.5:c.8G>C
|
ENSP00000443435.2:p.Gly3Ala
|
|
|
NM_000578.3:c.151G>C
|
NP_000569.3:p.Gly51Arg
|
|
|
XM_005246793.2:c.-51G>C
|
XP_005246850.1:n.-51G>C
|
|
|
XM_005246794.2:c.-278G>C
|
XP_005246851.1:n.-278G>C
|
|
|
XM_006712709.2:c.-278G>C
|
XP_006712772.1:n.-278G>C
|
|
|
XM_006712710.2:c.-155-904G>C
|
XP_006712773.1:n.-155-904G>C
|
|
|
XM_006712711.2:c.-174-904G>C
|
XP_006712774.1:n.-174-904G>C
|
|
|
XM_011511684.1:c.-286G>C
|
XP_011509986.1:n.-286G>C
|
|
|
XM_011511685.1:c.-286G>C
|
XP_011509987.1:n.-286G>C
|
|
|
XR_427107.1:n.314G>C
|
|
|
|
XR_427108.2:n.611G>C
|
|
|
|
XM_005246793.4:c.-51G>C
|
XP_005246850.1:n.-51G>C
|
|
|
XM_005246794.4:c.-278G>C
|
XP_005246851.1:n.-278G>C
|
|
|
XM_006712709.4:c.-278G>C
|
XP_006712772.1:n.-278G>C
|
|
|
XM_006712710.4:c.-155-904G>C
|
XP_006712773.1:n.-155-904G>C
|
|
|
XM_006712711.4:c.-174-904G>C
|
XP_006712774.1:n.-174-904G>C
|
|
|
XM_011511684.3:c.-286G>C
|
XP_011509986.1:n.-286G>C
|
|
|
XM_011511685.3:c.-286G>C
|
XP_011509987.1:n.-286G>C
|
|
|
XM_017004765.2:c.151-904G>C
|
XP_016860254.1:n.151-904G>C
|
|
|
XM_017004766.2:c.-51G>C
|
XP_016860255.1:n.-51G>C
|
|
|
XM_017004767.2:c.151G>C
|
XP_016860256.1:p.Gly51Arg
|
|
|
XR_427107.3:n.300G>C
|
|
|
|
XR_427108.4:n.611G>C
|
|
|
|
NM_000578.4:c.151G>C
MANE Select
|
NP_000569.3:p.Gly51Arg
|
|
