ENST00000373344.11:c.7272A>G
MANE Select
|
ENSP00000362441.4:p.Gln2424=
|
|
ENST00000675732.1:c.2370A>G
|
ENSP00000502598.1:p.Gln790=
|
|
ENST00000373344.9:c.7272A>G
|
ENSP00000362441.4:p.Gln2424=
|
|
ENST00000395603.7:c.7158A>G
|
ENSP00000378967.3:p.Gln2386=
|
|
ENST00000480283.5:c.*6900A>G
|
ENSP00000480196.1:n.*6900A>G
|
|
ENST00000623706.3:n.5592A>G
|
|
|
ENST00000624766.1:n.503A>G
|
|
|
NM_000489.4:c.7272A>G
|
NP_000480.3:p.Gln2424=
|
|
NM_138270.3:c.7158A>G
|
NP_612114.2:p.Gln2386=
|
|
XM_005262153.3:c.7269A>G
|
XP_005262210.2:p.Gln2423=
|
|
XM_005262154.3:c.7185A>G
|
XP_005262211.2:p.Gln2395=
|
|
XM_005262155.3:c.7155A>G
|
XP_005262212.2:p.Gln2385=
|
|
XM_005262156.3:c.7107A>G
|
XP_005262213.2:p.Gln2369=
|
|
XM_005262157.3:c.7068A>G
|
XP_005262214.2:p.Gln2356=
|
|
XM_006724666.2:c.7155A>G
|
XP_006724729.1:p.Gln2385=
|
|
XM_006724667.2:c.6993A>G
|
XP_006724730.1:p.Gln2331=
|
|
XR_938400.1:n.8864A>G
|
|
|
NM_000489.5:c.7272A>G
|
NP_000480.3:p.Gln2424=
|
|
XM_005262153.5:c.7269A>G
|
XP_005262210.2:p.Gln2423=
|
|
XM_005262154.5:c.7185A>G
|
XP_005262211.2:p.Gln2395=
|
|
XM_005262155.4:c.7155A>G
|
XP_005262212.2:p.Gln2385=
|
|
XM_005262156.4:c.7107A>G
|
XP_005262213.2:p.Gln2369=
|
|
XM_005262157.5:c.7068A>G
|
XP_005262214.2:p.Gln2356=
|
|
XM_006724666.4:c.7155A>G
|
XP_006724729.1:p.Gln2385=
|
|
XM_006724667.3:c.6993A>G
|
XP_006724730.1:p.Gln2331=
|
|
XM_017029601.2:c.7182A>G
|
XP_016885090.1:p.Gln2394=
|
|
XM_017029602.1:c.7152A>G
|
XP_016885091.1:p.Gln2384=
|
|
XM_017029603.1:c.7104A>G
|
XP_016885092.1:p.Gln2368=
|
|
XM_017029604.2:c.7071A>G
|
XP_016885093.1:p.Gln2357=
|
|
XM_017029605.1:c.7068A>G
|
XP_016885094.1:p.Gln2356=
|
|
XM_017029606.2:c.7041A>G
|
XP_016885095.1:p.Gln2347=
|
|
XM_017029607.2:c.7038A>G
|
XP_016885096.1:p.Gln2346=
|
|
XM_017029608.2:c.6990A>G
|
XP_016885097.1:p.Gln2330=
|
|
XM_017029609.1:c.6954A>G
|
XP_016885098.1:p.Gln2318=
|
|
XM_017029610.1:c.6951A>G
|
XP_016885099.1:p.Gln2317=
|
|
XM_017029611.1:c.6906A>G
|
XP_016885100.1:p.Gln2302=
|
|
XR_001755700.2:n.7571A>G
|
|
|
NM_138270.4:c.7158A>G
|
NP_612114.2:p.Gln2386=
|
|
NM_000489.6:c.7272A>G
MANE Select
|
NP_000480.3:p.Gln2424=
|
|
NM_138270.5:c.7158A>G
|
NP_612114.2:p.Gln2386=
|
|