ENST00000261304.7:c.1794G>T
MANE Select
|
ENSP00000261304.2:p.Trp598Cys
|
|
ENST00000261304.6:c.1794G>T
|
ENSP00000261304.2:p.Trp598Cys
|
|
ENST00000393568.8:c.1725G>T
|
ENSP00000377198.4:p.Trp575Cys
|
|
ENST00000393569.6:c.1716G>T
|
ENSP00000377199.2:p.Trp572Cys
|
|
ENST00000544807.6:c.1626G>T
|
ENSP00000437513.2:p.Trp542Cys
|
|
ENST00000555000.5:c.1161G>T
|
ENSP00000450472.1:p.Trp387Cys
|
|
ENST00000555179.1:c.330G>T
|
|
|
ENST00000557316.5:c.*1192G>T
|
ENSP00000452314.1:n.*1192G>T
|
|
NM_000153.3:c.1794G>T
|
NP_000144.2:p.Trp598Cys
|
|
NM_001201401.1:c.1725G>T
|
NP_001188330.1:p.Trp575Cys
|
|
NM_001201402.1:c.1716G>T
|
NP_001188331.1:p.Trp572Cys
|
|
XM_011536618.1:c.1626G>T
|
XP_011534920.1:p.Trp542Cys
|
|
XM_011536618.2:c.1626G>T
|
XP_011534920.1:p.Trp542Cys
|
|
NM_000153.4:c.1794G>T
MANE Select
|
NP_000144.2:p.Trp598Cys
|
|
NM_001201401.2:c.1725G>T
|
NP_001188330.1:p.Trp575Cys
|
|
NM_001201402.2:c.1716G>T
|
NP_001188331.1:p.Trp572Cys
|
|