ENST00000373344.11:c.7376T>C
MANE Select
|
ENSP00000362441.4:p.Met2459Thr
|
|
ENST00000675732.1:c.2474T>C
|
ENSP00000502598.1:p.Met825Thr
|
|
ENST00000373344.9:c.7376T>C
|
ENSP00000362441.4:p.Met2459Thr
|
|
ENST00000395603.7:c.7262T>C
|
ENSP00000378967.3:p.Met2421Thr
|
|
ENST00000480283.5:c.*7004T>C
|
ENSP00000480196.1:n.*7004T>C
|
|
ENST00000623706.3:n.5696T>C
|
|
|
NM_000489.4:c.7376T>C
|
NP_000480.3:p.Met2459Thr
|
|
NM_138270.3:c.7262T>C
|
NP_612114.2:p.Met2421Thr
|
|
XM_005262153.3:c.7373T>C
|
XP_005262210.2:p.Met2458Thr
|
|
XM_005262154.3:c.7289T>C
|
XP_005262211.2:p.Met2430Thr
|
|
XM_005262155.3:c.7259T>C
|
XP_005262212.2:p.Met2420Thr
|
|
XM_005262156.3:c.7211T>C
|
XP_005262213.2:p.Met2404Thr
|
|
XM_005262157.3:c.7172T>C
|
XP_005262214.2:p.Met2391Thr
|
|
XM_006724666.2:c.7259T>C
|
XP_006724729.1:p.Met2420Thr
|
|
XM_006724667.2:c.7097T>C
|
XP_006724730.1:p.Met2366Thr
|
|
XR_938400.1:n.8968T>C
|
|
|
NM_000489.5:c.7376T>C
|
NP_000480.3:p.Met2459Thr
|
|
XM_005262153.5:c.7373T>C
|
XP_005262210.2:p.Met2458Thr
|
|
XM_005262154.5:c.7289T>C
|
XP_005262211.2:p.Met2430Thr
|
|
XM_005262155.4:c.7259T>C
|
XP_005262212.2:p.Met2420Thr
|
|
XM_005262156.4:c.7211T>C
|
XP_005262213.2:p.Met2404Thr
|
|
XM_005262157.5:c.7172T>C
|
XP_005262214.2:p.Met2391Thr
|
|
XM_006724666.4:c.7259T>C
|
XP_006724729.1:p.Met2420Thr
|
|
XM_006724667.3:c.7097T>C
|
XP_006724730.1:p.Met2366Thr
|
|
XM_017029601.2:c.7286T>C
|
XP_016885090.1:p.Met2429Thr
|
|
XM_017029602.1:c.7256T>C
|
XP_016885091.1:p.Met2419Thr
|
|
XM_017029603.1:c.7208T>C
|
XP_016885092.1:p.Met2403Thr
|
|
XM_017029604.2:c.7175T>C
|
XP_016885093.1:p.Met2392Thr
|
|
XM_017029605.1:c.7172T>C
|
XP_016885094.1:p.Met2391Thr
|
|
XM_017029606.2:c.7145T>C
|
XP_016885095.1:p.Met2382Thr
|
|
XM_017029607.2:c.7142T>C
|
XP_016885096.1:p.Met2381Thr
|
|
XM_017029608.2:c.7094T>C
|
XP_016885097.1:p.Met2365Thr
|
|
XM_017029609.1:c.7058T>C
|
XP_016885098.1:p.Met2353Thr
|
|
XM_017029610.1:c.7055T>C
|
XP_016885099.1:p.Met2352Thr
|
|
XM_017029611.1:c.7010T>C
|
XP_016885100.1:p.Met2337Thr
|
|
XR_001755700.2:n.7675T>C
|
|
|
NM_138270.4:c.7262T>C
|
NP_612114.2:p.Met2421Thr
|
|
NM_000489.6:c.7376T>C
MANE Select
|
NP_000480.3:p.Met2459Thr
|
|
NM_138270.5:c.7262T>C
|
NP_612114.2:p.Met2421Thr
|
|