ENST00000373344.11:c.7290A>T
MANE Select
|
ENSP00000362441.4:p.Gln2430His
|
|
ENST00000675732.1:c.2388A>T
|
ENSP00000502598.1:p.Gln796His
|
|
ENST00000373344.9:c.7290A>T
|
ENSP00000362441.4:p.Gln2430His
|
|
ENST00000395603.7:c.7176A>T
|
ENSP00000378967.3:p.Gln2392His
|
|
ENST00000480283.5:c.*6918A>T
|
ENSP00000480196.1:n.*6918A>T
|
|
ENST00000623706.3:n.5610A>T
|
|
|
ENST00000624766.1:n.521A>T
|
|
|
NM_000489.4:c.7290A>T
|
NP_000480.3:p.Gln2430His
|
|
NM_138270.3:c.7176A>T
|
NP_612114.2:p.Gln2392His
|
|
XM_005262153.3:c.7287A>T
|
XP_005262210.2:p.Gln2429His
|
|
XM_005262154.3:c.7203A>T
|
XP_005262211.2:p.Gln2401His
|
|
XM_005262155.3:c.7173A>T
|
XP_005262212.2:p.Gln2391His
|
|
XM_005262156.3:c.7125A>T
|
XP_005262213.2:p.Gln2375His
|
|
XM_005262157.3:c.7086A>T
|
XP_005262214.2:p.Gln2362His
|
|
XM_006724666.2:c.7173A>T
|
XP_006724729.1:p.Gln2391His
|
|
XM_006724667.2:c.7011A>T
|
XP_006724730.1:p.Gln2337His
|
|
XR_938400.1:n.8882A>T
|
|
|
NM_000489.5:c.7290A>T
|
NP_000480.3:p.Gln2430His
|
|
XM_005262153.5:c.7287A>T
|
XP_005262210.2:p.Gln2429His
|
|
XM_005262154.5:c.7203A>T
|
XP_005262211.2:p.Gln2401His
|
|
XM_005262155.4:c.7173A>T
|
XP_005262212.2:p.Gln2391His
|
|
XM_005262156.4:c.7125A>T
|
XP_005262213.2:p.Gln2375His
|
|
XM_005262157.5:c.7086A>T
|
XP_005262214.2:p.Gln2362His
|
|
XM_006724666.4:c.7173A>T
|
XP_006724729.1:p.Gln2391His
|
|
XM_006724667.3:c.7011A>T
|
XP_006724730.1:p.Gln2337His
|
|
XM_017029601.2:c.7200A>T
|
XP_016885090.1:p.Gln2400His
|
|
XM_017029602.1:c.7170A>T
|
XP_016885091.1:p.Gln2390His
|
|
XM_017029603.1:c.7122A>T
|
XP_016885092.1:p.Gln2374His
|
|
XM_017029604.2:c.7089A>T
|
XP_016885093.1:p.Gln2363His
|
|
XM_017029605.1:c.7086A>T
|
XP_016885094.1:p.Gln2362His
|
|
XM_017029606.2:c.7059A>T
|
XP_016885095.1:p.Gln2353His
|
|
XM_017029607.2:c.7056A>T
|
XP_016885096.1:p.Gln2352His
|
|
XM_017029608.2:c.7008A>T
|
XP_016885097.1:p.Gln2336His
|
|
XM_017029609.1:c.6972A>T
|
XP_016885098.1:p.Gln2324His
|
|
XM_017029610.1:c.6969A>T
|
XP_016885099.1:p.Gln2323His
|
|
XM_017029611.1:c.6924A>T
|
XP_016885100.1:p.Gln2308His
|
|
XR_001755700.2:n.7589A>T
|
|
|
NM_138270.4:c.7176A>T
|
NP_612114.2:p.Gln2392His
|
|
NM_000489.6:c.7290A>T
MANE Select
|
NP_000480.3:p.Gln2430His
|
|
NM_138270.5:c.7176A>T
|
NP_612114.2:p.Gln2392His
|
|