ENST00000373344.11:c.4318A>T
MANE Select
|
ENSP00000362441.4:p.Ser1440Cys
|
|
ENST00000373344.9:c.4318A>T
|
ENSP00000362441.4:p.Ser1440Cys
|
|
ENST00000395603.7:c.4204A>T
|
ENSP00000378967.3:p.Ser1402Cys
|
|
ENST00000480283.5:c.*3946A>T
|
ENSP00000480196.1:n.*3946A>T
|
|
NM_000489.4:c.4318A>T
|
NP_000480.3:p.Ser1440Cys
|
|
NM_138270.3:c.4204A>T
|
NP_612114.2:p.Ser1402Cys
|
|
XM_005262153.3:c.4315A>T
|
XP_005262210.2:p.Ser1439Cys
|
|
XM_005262154.3:c.4231A>T
|
XP_005262211.2:p.Ser1411Cys
|
|
XM_005262155.3:c.4201A>T
|
XP_005262212.2:p.Ser1401Cys
|
|
XM_005262156.3:c.4153A>T
|
XP_005262213.2:p.Ser1385Cys
|
|
XM_005262157.3:c.4114A>T
|
XP_005262214.2:p.Ser1372Cys
|
|
XM_006724666.2:c.4201A>T
|
XP_006724729.1:p.Ser1401Cys
|
|
XM_006724667.2:c.4039A>T
|
XP_006724730.1:p.Ser1347Cys
|
|
XM_006724668.2:c.4318A>T
|
XP_006724731.1:p.Ser1440Cys
|
|
XR_938400.1:n.4586A>T
|
|
|
NM_000489.5:c.4318A>T
|
NP_000480.3:p.Ser1440Cys
|
|
XM_005262153.5:c.4315A>T
|
XP_005262210.2:p.Ser1439Cys
|
|
XM_005262154.5:c.4231A>T
|
XP_005262211.2:p.Ser1411Cys
|
|
XM_005262155.4:c.4201A>T
|
XP_005262212.2:p.Ser1401Cys
|
|
XM_005262156.4:c.4153A>T
|
XP_005262213.2:p.Ser1385Cys
|
|
XM_005262157.5:c.4114A>T
|
XP_005262214.2:p.Ser1372Cys
|
|
XM_006724666.4:c.4201A>T
|
XP_006724729.1:p.Ser1401Cys
|
|
XM_006724667.3:c.4039A>T
|
XP_006724730.1:p.Ser1347Cys
|
|
XM_006724668.3:c.4318A>T
|
XP_006724731.1:p.Ser1440Cys
|
|
XM_017029601.2:c.4228A>T
|
XP_016885090.1:p.Ser1410Cys
|
|
XM_017029602.1:c.4198A>T
|
XP_016885091.1:p.Ser1400Cys
|
|
XM_017029603.1:c.4150A>T
|
XP_016885092.1:p.Ser1384Cys
|
|
XM_017029604.2:c.4117A>T
|
XP_016885093.1:p.Ser1373Cys
|
|
XM_017029605.1:c.4114A>T
|
XP_016885094.1:p.Ser1372Cys
|
|
XM_017029606.2:c.4087A>T
|
XP_016885095.1:p.Ser1363Cys
|
|
XM_017029607.2:c.4084A>T
|
XP_016885096.1:p.Ser1362Cys
|
|
XM_017029608.2:c.4036A>T
|
XP_016885097.1:p.Ser1346Cys
|
|
XM_017029609.1:c.4000A>T
|
XP_016885098.1:p.Ser1334Cys
|
|
XM_017029610.1:c.3997A>T
|
XP_016885099.1:p.Ser1333Cys
|
|
XM_017029611.1:c.3952A>T
|
XP_016885100.1:p.Ser1318Cys
|
|
XR_001755700.2:n.4543A>T
|
|
|
NM_138270.4:c.4204A>T
|
NP_612114.2:p.Ser1402Cys
|
|
NM_000489.6:c.4318A>T
MANE Select
|
NP_000480.3:p.Ser1440Cys
|
|
NM_138270.5:c.4204A>T
|
NP_612114.2:p.Ser1402Cys
|
|