ENST00000373344.11:c.7304A>T
MANE Select
|
ENSP00000362441.4:p.His2435Leu
|
|
ENST00000675732.1:c.2402A>T
|
ENSP00000502598.1:p.His801Leu
|
|
ENST00000373344.9:c.7304A>T
|
ENSP00000362441.4:p.His2435Leu
|
|
ENST00000395603.7:c.7190A>T
|
ENSP00000378967.3:p.His2397Leu
|
|
ENST00000480283.5:c.*6932A>T
|
ENSP00000480196.1:n.*6932A>T
|
|
ENST00000623706.3:n.5624A>T
|
|
|
ENST00000624766.1:n.535A>T
|
|
|
NM_000489.4:c.7304A>T
|
NP_000480.3:p.His2435Leu
|
|
NM_138270.3:c.7190A>T
|
NP_612114.2:p.His2397Leu
|
|
XM_005262153.3:c.7301A>T
|
XP_005262210.2:p.His2434Leu
|
|
XM_005262154.3:c.7217A>T
|
XP_005262211.2:p.His2406Leu
|
|
XM_005262155.3:c.7187A>T
|
XP_005262212.2:p.His2396Leu
|
|
XM_005262156.3:c.7139A>T
|
XP_005262213.2:p.His2380Leu
|
|
XM_005262157.3:c.7100A>T
|
XP_005262214.2:p.His2367Leu
|
|
XM_006724666.2:c.7187A>T
|
XP_006724729.1:p.His2396Leu
|
|
XM_006724667.2:c.7025A>T
|
XP_006724730.1:p.His2342Leu
|
|
XR_938400.1:n.8896A>T
|
|
|
NM_000489.5:c.7304A>T
|
NP_000480.3:p.His2435Leu
|
|
XM_005262153.5:c.7301A>T
|
XP_005262210.2:p.His2434Leu
|
|
XM_005262154.5:c.7217A>T
|
XP_005262211.2:p.His2406Leu
|
|
XM_005262155.4:c.7187A>T
|
XP_005262212.2:p.His2396Leu
|
|
XM_005262156.4:c.7139A>T
|
XP_005262213.2:p.His2380Leu
|
|
XM_005262157.5:c.7100A>T
|
XP_005262214.2:p.His2367Leu
|
|
XM_006724666.4:c.7187A>T
|
XP_006724729.1:p.His2396Leu
|
|
XM_006724667.3:c.7025A>T
|
XP_006724730.1:p.His2342Leu
|
|
XM_017029601.2:c.7214A>T
|
XP_016885090.1:p.His2405Leu
|
|
XM_017029602.1:c.7184A>T
|
XP_016885091.1:p.His2395Leu
|
|
XM_017029603.1:c.7136A>T
|
XP_016885092.1:p.His2379Leu
|
|
XM_017029604.2:c.7103A>T
|
XP_016885093.1:p.His2368Leu
|
|
XM_017029605.1:c.7100A>T
|
XP_016885094.1:p.His2367Leu
|
|
XM_017029606.2:c.7073A>T
|
XP_016885095.1:p.His2358Leu
|
|
XM_017029607.2:c.7070A>T
|
XP_016885096.1:p.His2357Leu
|
|
XM_017029608.2:c.7022A>T
|
XP_016885097.1:p.His2341Leu
|
|
XM_017029609.1:c.6986A>T
|
XP_016885098.1:p.His2329Leu
|
|
XM_017029610.1:c.6983A>T
|
XP_016885099.1:p.His2328Leu
|
|
XM_017029611.1:c.6938A>T
|
XP_016885100.1:p.His2313Leu
|
|
XR_001755700.2:n.7603A>T
|
|
|
NM_138270.4:c.7190A>T
|
NP_612114.2:p.His2397Leu
|
|
NM_000489.6:c.7304A>T
MANE Select
|
NP_000480.3:p.His2435Leu
|
|
NM_138270.5:c.7190A>T
|
NP_612114.2:p.His2397Leu
|
|