ENST00000373344.11:c.7359G>C
MANE Select
|
ENSP00000362441.4:p.Gln2453His
|
|
ENST00000675732.1:c.2457G>C
|
ENSP00000502598.1:p.Gln819His
|
|
ENST00000373344.9:c.7359G>C
|
ENSP00000362441.4:p.Gln2453His
|
|
ENST00000395603.7:c.7245G>C
|
ENSP00000378967.3:p.Gln2415His
|
|
ENST00000480283.5:c.*6987G>C
|
ENSP00000480196.1:n.*6987G>C
|
|
ENST00000623706.3:n.5679G>C
|
|
|
NM_000489.4:c.7359G>C
|
NP_000480.3:p.Gln2453His
|
|
NM_138270.3:c.7245G>C
|
NP_612114.2:p.Gln2415His
|
|
XM_005262153.3:c.7356G>C
|
XP_005262210.2:p.Gln2452His
|
|
XM_005262154.3:c.7272G>C
|
XP_005262211.2:p.Gln2424His
|
|
XM_005262155.3:c.7242G>C
|
XP_005262212.2:p.Gln2414His
|
|
XM_005262156.3:c.7194G>C
|
XP_005262213.2:p.Gln2398His
|
|
XM_005262157.3:c.7155G>C
|
XP_005262214.2:p.Gln2385His
|
|
XM_006724666.2:c.7242G>C
|
XP_006724729.1:p.Gln2414His
|
|
XM_006724667.2:c.7080G>C
|
XP_006724730.1:p.Gln2360His
|
|
XR_938400.1:n.8951G>C
|
|
|
NM_000489.5:c.7359G>C
|
NP_000480.3:p.Gln2453His
|
|
XM_005262153.5:c.7356G>C
|
XP_005262210.2:p.Gln2452His
|
|
XM_005262154.5:c.7272G>C
|
XP_005262211.2:p.Gln2424His
|
|
XM_005262155.4:c.7242G>C
|
XP_005262212.2:p.Gln2414His
|
|
XM_005262156.4:c.7194G>C
|
XP_005262213.2:p.Gln2398His
|
|
XM_005262157.5:c.7155G>C
|
XP_005262214.2:p.Gln2385His
|
|
XM_006724666.4:c.7242G>C
|
XP_006724729.1:p.Gln2414His
|
|
XM_006724667.3:c.7080G>C
|
XP_006724730.1:p.Gln2360His
|
|
XM_017029601.2:c.7269G>C
|
XP_016885090.1:p.Gln2423His
|
|
XM_017029602.1:c.7239G>C
|
XP_016885091.1:p.Gln2413His
|
|
XM_017029603.1:c.7191G>C
|
XP_016885092.1:p.Gln2397His
|
|
XM_017029604.2:c.7158G>C
|
XP_016885093.1:p.Gln2386His
|
|
XM_017029605.1:c.7155G>C
|
XP_016885094.1:p.Gln2385His
|
|
XM_017029606.2:c.7128G>C
|
XP_016885095.1:p.Gln2376His
|
|
XM_017029607.2:c.7125G>C
|
XP_016885096.1:p.Gln2375His
|
|
XM_017029608.2:c.7077G>C
|
XP_016885097.1:p.Gln2359His
|
|
XM_017029609.1:c.7041G>C
|
XP_016885098.1:p.Gln2347His
|
|
XM_017029610.1:c.7038G>C
|
XP_016885099.1:p.Gln2346His
|
|
XM_017029611.1:c.6993G>C
|
XP_016885100.1:p.Gln2331His
|
|
XR_001755700.2:n.7658G>C
|
|
|
NM_138270.4:c.7245G>C
|
NP_612114.2:p.Gln2415His
|
|
NM_000489.6:c.7359G>C
MANE Select
|
NP_000480.3:p.Gln2453His
|
|
NM_138270.5:c.7245G>C
|
NP_612114.2:p.Gln2415His
|
|