ENST00000292408.9:c.1285A>T
MANE Select
|
ENSP00000292408.4:p.Ser429Cys
|
|
ENST00000292408.8:c.1285A>T
|
ENSP00000292408.4:p.Ser429Cys
|
|
ENST00000393637.5:c.1165A>T
|
ENSP00000377254.1:p.Ser389Cys
|
|
ENST00000393648.6:c.1131A>T
|
ENSP00000377259.2:p.Gln377His
|
|
ENST00000502906.5:c.1285A>T
|
ENSP00000424960.1:p.Ser429Cys
|
|
ENST00000508139.1:n.663A>T
|
|
|
ENST00000511076.1:c.179A>T
|
|
|
NM_001291980.1:c.1131A>T
|
NP_001278909.1:p.Gln377His
|
|
NM_002011.4:c.1285A>T
|
NP_002002.3:p.Ser429Cys
|
|
NM_022963.3:c.1165A>T
|
NP_075252.2:p.Ser389Cys
|
|
NM_213647.2:c.1285A>T
|
NP_998812.1:p.Ser429Cys
|
|
XM_005265838.2:c.1285A>T
|
XP_005265895.1:p.Ser429Cys
|
|
XM_011534464.1:c.1378A>T
|
XP_011532766.1:p.Ser460Cys
|
|
XM_011534465.1:c.967A>T
|
XP_011532767.1:p.Ser323Cys
|
|
XR_941090.1:n.1330A>T
|
|
|
NM_001354984.1:c.1285A>T
|
NP_001341913.1:p.Ser429Cys
|
|
NM_213647.3:c.1285A>T
MANE Select
|
NP_998812.1:p.Ser429Cys
|
|
NM_001291980.2:c.1131A>T
|
NP_001278909.1:p.Gln377His
|
|
NM_001354984.2:c.1285A>T
|
NP_001341913.1:p.Ser429Cys
|
|
NM_002011.5:c.1285A>T
|
NP_002002.3:p.Ser429Cys
|
|