ENST00000320393.9:c.1148A>T
MANE Select
|
ENSP00000318351.5:p.Tyr383Phe
|
|
ENST00000320393.8:c.1148A>T
|
ENSP00000318351.5:p.Tyr383Phe
|
|
ENST00000356489.9:c.1148A>T
|
ENSP00000348880.5:p.Tyr383Phe
|
|
ENST00000491328.1:n.203A>T
|
|
|
NM_000056.3:c.1148A>T
|
NP_000047.1:p.Tyr383Phe
|
|
NM_183050.2:c.1148A>T
|
NP_898871.1:p.Tyr383Phe
|
|
XM_006715542.2:c.938A>T
|
XP_006715605.1:p.Tyr313Phe
|
|
XM_011536024.1:c.*154A>T
|
XP_011534326.1:n.*154A>T
|
|
XM_011536026.1:c.938A>T
|
XP_011534328.1:p.Tyr313Phe
|
|
NM_000056.4:c.1148A>T
|
NP_000047.1:p.Tyr383Phe
|
|
NM_001318975.1:c.938A>T
|
NP_001305904.1:p.Tyr313Phe
|
|
NM_183050.3:c.1148A>T
|
NP_898871.1:p.Tyr383Phe
|
|
NR_134945.1:n.1326A>T
|
|
|
XM_011536024.3:c.*154A>T
|
XP_011534326.1:n.*154A>T
|
|
XR_001743546.2:n.1068+70552A>T
|
|
|
XR_001743547.2:n.1068+70552A>T
|
|
|
XR_001743548.2:n.1068+70552A>T
|
|
|
XR_001743549.2:n.1068+70552A>T
|
|
|
XR_002956292.1:n.1068+70552A>T
|
|
|
NM_183050.4:c.1148A>T
MANE Select
|
NP_898871.1:p.Tyr383Phe
|
|
NR_134945.2:n.1265A>T
|
|
|
NM_000056.5:c.1148A>T
|
NP_000047.1:p.Tyr383Phe
|
|