ENST00000304895.9:c.1877A>T
MANE Select
|
ENSP00000302728.4:p.Tyr626Phe
|
|
ENST00000304895.8:c.1877A>T
|
ENSP00000302728.4:p.Tyr626Phe
|
|
ENST00000421103.5:c.1439A>T
|
ENSP00000391390.1:p.Tyr480Phe
|
|
ENST00000430730.5:c.*1144A>T
|
ENSP00000411859.1:n.*1144A>T
|
|
ENST00000447929.5:c.*1257A>T
|
ENSP00000411262.1:n.*1257A>T
|
|
ENST00000466883.5:n.2267A>T
|
|
|
NM_000181.3:c.1877A>T
|
NP_000172.2:p.Tyr626Phe
|
|
NM_001284290.1:c.1439A>T
|
NP_001271219.1:p.Tyr480Phe
|
|
NM_001293104.1:c.1307A>T
|
NP_001280033.1:p.Tyr436Phe
|
|
NM_001293105.1:c.1220A>T
|
NP_001280034.1:p.Tyr407Phe
|
|
NR_120531.1:n.1923A>T
|
|
|
XM_005250297.3:c.1724A>T
|
XP_005250354.1:p.Tyr575Phe
|
|
XM_011516113.1:c.1376A>T
|
XP_011514415.1:p.Tyr459Phe
|
|
XM_011516114.1:c.1205A>T
|
XP_011514416.1:p.Tyr402Phe
|
|
XM_005250297.4:c.1724A>T
|
XP_005250354.1:p.Tyr575Phe
|
|
XM_011516114.2:c.1205A>T
|
XP_011514416.1:p.Tyr402Phe
|
|
XM_017012091.1:c.1223A>T
|
XP_016867580.1:p.Tyr408Phe
|
|
XM_017012092.1:c.1154A>T
|
XP_016867581.1:p.Tyr385Phe
|
|
XM_017012093.2:c.1052A>T
|
XP_016867582.1:p.Tyr351Phe
|
|
XR_001744658.2:n.1684A>T
|
|
|
XR_001744659.2:n.1797A>T
|
|
|
XR_001744660.2:n.1729A>T
|
|
|
XR_001744661.2:n.1644A>T
|
|
|
XR_927461.3:n.1882A>T
|
|
|
NM_000181.4:c.1877A>T
MANE Select
|
NP_000172.2:p.Tyr626Phe
|
|
NM_001284290.2:c.1439A>T
|
NP_001271219.1:p.Tyr480Phe
|
|
NM_001293104.2:c.1307A>T
|
NP_001280033.1:p.Tyr436Phe
|
|
NM_001293105.2:c.1220A>T
|
NP_001280034.1:p.Tyr407Phe
|
|
NR_120531.2:n.1822A>T
|
|
|