ENST00000373344.11:c.6251A>T
MANE Select
|
ENSP00000362441.4:p.Tyr2084Phe
|
|
ENST00000636152.1:n.86A>T
|
|
|
ENST00000675732.1:c.1349A>T
|
ENSP00000502598.1:p.Tyr450Phe
|
|
ENST00000373344.9:c.6251A>T
|
ENSP00000362441.4:p.Tyr2084Phe
|
|
ENST00000395603.7:c.6137A>T
|
ENSP00000378967.3:p.Tyr2046Phe
|
|
ENST00000480283.5:c.*5879A>T
|
ENSP00000480196.1:n.*5879A>T
|
|
ENST00000623316.1:c.735A>T
|
|
|
ENST00000623706.3:n.3321A>T
|
|
|
NM_000489.4:c.6251A>T
|
NP_000480.3:p.Tyr2084Phe
|
|
NM_138270.3:c.6137A>T
|
NP_612114.2:p.Tyr2046Phe
|
|
XM_005262153.3:c.6248A>T
|
XP_005262210.2:p.Tyr2083Phe
|
|
XM_005262154.3:c.6164A>T
|
XP_005262211.2:p.Tyr2055Phe
|
|
XM_005262155.3:c.6134A>T
|
XP_005262212.2:p.Tyr2045Phe
|
|
XM_005262156.3:c.6086A>T
|
XP_005262213.2:p.Tyr2029Phe
|
|
XM_005262157.3:c.6047A>T
|
XP_005262214.2:p.Tyr2016Phe
|
|
XM_006724666.2:c.6134A>T
|
XP_006724729.1:p.Tyr2045Phe
|
|
XM_006724667.2:c.5972A>T
|
XP_006724730.1:p.Tyr1991Phe
|
|
XR_938400.1:n.6593A>T
|
|
|
NM_000489.5:c.6251A>T
|
NP_000480.3:p.Tyr2084Phe
|
|
XM_005262153.5:c.6248A>T
|
XP_005262210.2:p.Tyr2083Phe
|
|
XM_005262154.5:c.6164A>T
|
XP_005262211.2:p.Tyr2055Phe
|
|
XM_005262155.4:c.6134A>T
|
XP_005262212.2:p.Tyr2045Phe
|
|
XM_005262156.4:c.6086A>T
|
XP_005262213.2:p.Tyr2029Phe
|
|
XM_005262157.5:c.6047A>T
|
XP_005262214.2:p.Tyr2016Phe
|
|
XM_006724666.4:c.6134A>T
|
XP_006724729.1:p.Tyr2045Phe
|
|
XM_006724667.3:c.5972A>T
|
XP_006724730.1:p.Tyr1991Phe
|
|
XM_017029601.2:c.6161A>T
|
XP_016885090.1:p.Tyr2054Phe
|
|
XM_017029602.1:c.6131A>T
|
XP_016885091.1:p.Tyr2044Phe
|
|
XM_017029603.1:c.6083A>T
|
XP_016885092.1:p.Tyr2028Phe
|
|
XM_017029604.2:c.6050A>T
|
XP_016885093.1:p.Tyr2017Phe
|
|
XM_017029605.1:c.6047A>T
|
XP_016885094.1:p.Tyr2016Phe
|
|
XM_017029606.2:c.6020A>T
|
XP_016885095.1:p.Tyr2007Phe
|
|
XM_017029607.2:c.6017A>T
|
XP_016885096.1:p.Tyr2006Phe
|
|
XM_017029608.2:c.5969A>T
|
XP_016885097.1:p.Tyr1990Phe
|
|
XM_017029609.1:c.5933A>T
|
XP_016885098.1:p.Tyr1978Phe
|
|
XM_017029610.1:c.5930A>T
|
XP_016885099.1:p.Tyr1977Phe
|
|
XM_017029611.1:c.5885A>T
|
XP_016885100.1:p.Tyr1962Phe
|
|
XR_001755700.2:n.6550A>T
|
|
|
NM_138270.4:c.6137A>T
|
NP_612114.2:p.Tyr2046Phe
|
|
NM_000489.6:c.6251A>T
MANE Select
|
NP_000480.3:p.Tyr2084Phe
|
|
NM_138270.5:c.6137A>T
|
NP_612114.2:p.Tyr2046Phe
|
|