ENST00000373344.11:c.7155A>G
MANE Select
|
ENSP00000362441.4:p.Lys2385=
|
|
ENST00000675732.1:c.2253A>G
|
ENSP00000502598.1:p.Lys751=
|
|
ENST00000373344.9:c.7155A>G
|
ENSP00000362441.4:p.Lys2385=
|
|
ENST00000395603.7:c.7041A>G
|
ENSP00000378967.3:p.Lys2347=
|
|
ENST00000480283.5:c.*6783A>G
|
ENSP00000480196.1:n.*6783A>G
|
|
ENST00000623706.3:n.5475A>G
|
|
|
ENST00000624766.1:n.386A>G
|
|
|
NM_000489.4:c.7155A>G
|
NP_000480.3:p.Lys2385=
|
|
NM_138270.3:c.7041A>G
|
NP_612114.2:p.Lys2347=
|
|
XM_005262153.3:c.7152A>G
|
XP_005262210.2:p.Lys2384=
|
|
XM_005262154.3:c.7068A>G
|
XP_005262211.2:p.Lys2356=
|
|
XM_005262155.3:c.7038A>G
|
XP_005262212.2:p.Lys2346=
|
|
XM_005262156.3:c.6990A>G
|
XP_005262213.2:p.Lys2330=
|
|
XM_005262157.3:c.6951A>G
|
XP_005262214.2:p.Lys2317=
|
|
XM_006724666.2:c.7038A>G
|
XP_006724729.1:p.Lys2346=
|
|
XM_006724667.2:c.6876A>G
|
XP_006724730.1:p.Lys2292=
|
|
XR_938400.1:n.8747A>G
|
|
|
NM_000489.5:c.7155A>G
|
NP_000480.3:p.Lys2385=
|
|
XM_005262153.5:c.7152A>G
|
XP_005262210.2:p.Lys2384=
|
|
XM_005262154.5:c.7068A>G
|
XP_005262211.2:p.Lys2356=
|
|
XM_005262155.4:c.7038A>G
|
XP_005262212.2:p.Lys2346=
|
|
XM_005262156.4:c.6990A>G
|
XP_005262213.2:p.Lys2330=
|
|
XM_005262157.5:c.6951A>G
|
XP_005262214.2:p.Lys2317=
|
|
XM_006724666.4:c.7038A>G
|
XP_006724729.1:p.Lys2346=
|
|
XM_006724667.3:c.6876A>G
|
XP_006724730.1:p.Lys2292=
|
|
XM_017029601.2:c.7065A>G
|
XP_016885090.1:p.Lys2355=
|
|
XM_017029602.1:c.7035A>G
|
XP_016885091.1:p.Lys2345=
|
|
XM_017029603.1:c.6987A>G
|
XP_016885092.1:p.Lys2329=
|
|
XM_017029604.2:c.6954A>G
|
XP_016885093.1:p.Lys2318=
|
|
XM_017029605.1:c.6951A>G
|
XP_016885094.1:p.Lys2317=
|
|
XM_017029606.2:c.6924A>G
|
XP_016885095.1:p.Lys2308=
|
|
XM_017029607.2:c.6921A>G
|
XP_016885096.1:p.Lys2307=
|
|
XM_017029608.2:c.6873A>G
|
XP_016885097.1:p.Lys2291=
|
|
XM_017029609.1:c.6837A>G
|
XP_016885098.1:p.Lys2279=
|
|
XM_017029610.1:c.6834A>G
|
XP_016885099.1:p.Lys2278=
|
|
XM_017029611.1:c.6789A>G
|
XP_016885100.1:p.Lys2263=
|
|
XR_001755700.2:n.7454A>G
|
|
|
NM_138270.4:c.7041A>G
|
NP_612114.2:p.Lys2347=
|
|
NM_000489.6:c.7155A>G
MANE Select
|
NP_000480.3:p.Lys2385=
|
|
NM_138270.5:c.7041A>G
|
NP_612114.2:p.Lys2347=
|
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