ENST00000373344.11:c.7153A>T
MANE Select
|
ENSP00000362441.4:p.Lys2385Ter
|
|
ENST00000675732.1:c.2251A>T
|
ENSP00000502598.1:p.Lys751Ter
|
|
ENST00000373344.9:c.7153A>T
|
ENSP00000362441.4:p.Lys2385Ter
|
|
ENST00000395603.7:c.7039A>T
|
ENSP00000378967.3:p.Lys2347Ter
|
|
ENST00000480283.5:c.*6781A>T
|
ENSP00000480196.1:n.*6781A>T
|
|
ENST00000623706.3:n.5473A>T
|
|
|
ENST00000624766.1:n.384A>T
|
|
|
NM_000489.4:c.7153A>T
|
NP_000480.3:p.Lys2385Ter
|
|
NM_138270.3:c.7039A>T
|
NP_612114.2:p.Lys2347Ter
|
|
XM_005262153.3:c.7150A>T
|
XP_005262210.2:p.Lys2384Ter
|
|
XM_005262154.3:c.7066A>T
|
XP_005262211.2:p.Lys2356Ter
|
|
XM_005262155.3:c.7036A>T
|
XP_005262212.2:p.Lys2346Ter
|
|
XM_005262156.3:c.6988A>T
|
XP_005262213.2:p.Lys2330Ter
|
|
XM_005262157.3:c.6949A>T
|
XP_005262214.2:p.Lys2317Ter
|
|
XM_006724666.2:c.7036A>T
|
XP_006724729.1:p.Lys2346Ter
|
|
XM_006724667.2:c.6874A>T
|
XP_006724730.1:p.Lys2292Ter
|
|
XR_938400.1:n.8745A>T
|
|
|
NM_000489.5:c.7153A>T
|
NP_000480.3:p.Lys2385Ter
|
|
XM_005262153.5:c.7150A>T
|
XP_005262210.2:p.Lys2384Ter
|
|
XM_005262154.5:c.7066A>T
|
XP_005262211.2:p.Lys2356Ter
|
|
XM_005262155.4:c.7036A>T
|
XP_005262212.2:p.Lys2346Ter
|
|
XM_005262156.4:c.6988A>T
|
XP_005262213.2:p.Lys2330Ter
|
|
XM_005262157.5:c.6949A>T
|
XP_005262214.2:p.Lys2317Ter
|
|
XM_006724666.4:c.7036A>T
|
XP_006724729.1:p.Lys2346Ter
|
|
XM_006724667.3:c.6874A>T
|
XP_006724730.1:p.Lys2292Ter
|
|
XM_017029601.2:c.7063A>T
|
XP_016885090.1:p.Lys2355Ter
|
|
XM_017029602.1:c.7033A>T
|
XP_016885091.1:p.Lys2345Ter
|
|
XM_017029603.1:c.6985A>T
|
XP_016885092.1:p.Lys2329Ter
|
|
XM_017029604.2:c.6952A>T
|
XP_016885093.1:p.Lys2318Ter
|
|
XM_017029605.1:c.6949A>T
|
XP_016885094.1:p.Lys2317Ter
|
|
XM_017029606.2:c.6922A>T
|
XP_016885095.1:p.Lys2308Ter
|
|
XM_017029607.2:c.6919A>T
|
XP_016885096.1:p.Lys2307Ter
|
|
XM_017029608.2:c.6871A>T
|
XP_016885097.1:p.Lys2291Ter
|
|
XM_017029609.1:c.6835A>T
|
XP_016885098.1:p.Lys2279Ter
|
|
XM_017029610.1:c.6832A>T
|
XP_016885099.1:p.Lys2278Ter
|
|
XM_017029611.1:c.6787A>T
|
XP_016885100.1:p.Lys2263Ter
|
|
XR_001755700.2:n.7452A>T
|
|
|
NM_138270.4:c.7039A>T
|
NP_612114.2:p.Lys2347Ter
|
|
NM_000489.6:c.7153A>T
MANE Select
|
NP_000480.3:p.Lys2385Ter
|
|
NM_138270.5:c.7039A>T
|
NP_612114.2:p.Lys2347Ter
|
|