ENST00000373344.11:c.7162G=
MANE Select
|
ENSP00000362441.4:p.Glu2388=
|
|
ENST00000675732.1:c.2260G=
|
ENSP00000502598.1:p.Glu754=
|
|
ENST00000373344.9:c.7162G=
|
ENSP00000362441.4:p.Glu2388=
|
|
ENST00000395603.7:c.7048G=
|
ENSP00000378967.3:p.Glu2350=
|
|
ENST00000480283.5:c.*6790G=
|
ENSP00000480196.1:n.*6790G=
|
|
ENST00000623706.3:n.5482G=
|
|
|
ENST00000624766.1:n.393G=
|
|
|
NM_000489.4:c.7162G=
|
NP_000480.3:p.Glu2388=
|
|
NM_138270.3:c.7048G=
|
NP_612114.2:p.Glu2350=
|
|
XM_005262153.3:c.7159G=
|
XP_005262210.2:p.Glu2387=
|
|
XM_005262154.3:c.7075G=
|
XP_005262211.2:p.Glu2359=
|
|
XM_005262155.3:c.7045G=
|
XP_005262212.2:p.Glu2349=
|
|
XM_005262156.3:c.6997G=
|
XP_005262213.2:p.Glu2333=
|
|
XM_005262157.3:c.6958G=
|
XP_005262214.2:p.Glu2320=
|
|
XM_006724666.2:c.7045G=
|
XP_006724729.1:p.Glu2349=
|
|
XM_006724667.2:c.6883G=
|
XP_006724730.1:p.Glu2295=
|
|
XR_938400.1:n.8754G=
|
|
|
NM_000489.5:c.7162G=
|
NP_000480.3:p.Glu2388=
|
|
XM_005262153.5:c.7159G=
|
XP_005262210.2:p.Glu2387=
|
|
XM_005262154.5:c.7075G=
|
XP_005262211.2:p.Glu2359=
|
|
XM_005262155.4:c.7045G=
|
XP_005262212.2:p.Glu2349=
|
|
XM_005262156.4:c.6997G=
|
XP_005262213.2:p.Glu2333=
|
|
XM_005262157.5:c.6958G=
|
XP_005262214.2:p.Glu2320=
|
|
XM_006724666.4:c.7045G=
|
XP_006724729.1:p.Glu2349=
|
|
XM_006724667.3:c.6883G=
|
XP_006724730.1:p.Glu2295=
|
|
XM_017029601.2:c.7072G=
|
XP_016885090.1:p.Glu2358=
|
|
XM_017029602.1:c.7042G=
|
XP_016885091.1:p.Glu2348=
|
|
XM_017029603.1:c.6994G=
|
XP_016885092.1:p.Glu2332=
|
|
XM_017029604.2:c.6961G=
|
XP_016885093.1:p.Glu2321=
|
|
XM_017029605.1:c.6958G=
|
XP_016885094.1:p.Glu2320=
|
|
XM_017029606.2:c.6931G=
|
XP_016885095.1:p.Glu2311=
|
|
XM_017029607.2:c.6928G=
|
XP_016885096.1:p.Glu2310=
|
|
XM_017029608.2:c.6880G=
|
XP_016885097.1:p.Glu2294=
|
|
XM_017029609.1:c.6844G=
|
XP_016885098.1:p.Glu2282=
|
|
XM_017029610.1:c.6841G=
|
XP_016885099.1:p.Glu2281=
|
|
XM_017029611.1:c.6796G=
|
XP_016885100.1:p.Glu2266=
|
|
XR_001755700.2:n.7461G=
|
|
|
NM_138270.4:c.7048G=
|
NP_612114.2:p.Glu2350=
|
|
NM_000489.6:c.7162G=
MANE Select
|
NP_000480.3:p.Glu2388=
|
|
NM_138270.5:c.7048G=
|
NP_612114.2:p.Glu2350=
|
|