ENST00000264380.9:c.3389C>A
MANE Select
|
ENSP00000264380.4:p.Ser1130Ter
|
|
ENST00000264380.8:c.3389C>A
|
ENSP00000264380.4:p.Ser1130Ter
|
|
ENST00000452564.1:c.3221C>A
|
ENSP00000405736.1:p.Ser1074Ter
|
|
NM_015040.3:c.3389C>A
|
NP_055855.2:p.Ser1130Ter
|
|
XM_011510778.1:c.3425C>A
|
XP_011509080.1:p.Ser1142Ter
|
|
XM_011510779.1:c.3425C>A
|
XP_011509081.1:p.Ser1142Ter
|
|
XM_011510780.1:c.3422C>A
|
XP_011509082.1:p.Ser1141Ter
|
|
XM_011510781.1:c.3407C>A
|
XP_011509083.1:p.Ser1136Ter
|
|
XM_011510782.1:c.3425C>A
|
XP_011509084.1:p.Ser1142Ter
|
|
XM_011510783.1:c.3257C>A
|
XP_011509085.1:p.Ser1086Ter
|
|
XM_011510784.1:c.3254C>A
|
XP_011509086.1:p.Ser1085Ter
|
|
XM_011510785.1:c.3239C>A
|
XP_011509087.1:p.Ser1080Ter
|
|
XM_011510786.1:c.3134C>A
|
XP_011509088.1:p.Ser1045Ter
|
|
XM_011510787.1:c.3131C>A
|
XP_011509089.1:p.Ser1044Ter
|
|
XM_011510788.1:c.3098C>A
|
XP_011509090.1:p.Ser1033Ter
|
|
XM_011510789.1:c.2948C>A
|
XP_011509091.1:p.Ser983Ter
|
|
XM_011510790.1:c.2432C>A
|
XP_011509092.1:p.Ser811Ter
|
|
XM_011510791.1:c.2432C>A
|
XP_011509093.1:p.Ser811Ter
|
|
XM_011510792.1:c.3425C>A
|
XP_011509094.1:p.Ser1142Ter
|
|
XR_922888.1:n.3562C>A
|
|
|
XM_011510778.3:c.3425C>A
|
XP_011509080.1:p.Ser1142Ter
|
|
XM_011510779.2:c.3425C>A
|
XP_011509081.1:p.Ser1142Ter
|
|
XM_011510780.2:c.3422C>A
|
XP_011509082.1:p.Ser1141Ter
|
|
XM_011510781.3:c.3407C>A
|
XP_011509083.1:p.Ser1136Ter
|
|
XM_011510782.3:c.3425C>A
|
XP_011509084.1:p.Ser1142Ter
|
|
XM_011510783.3:c.3257C>A
|
XP_011509085.1:p.Ser1086Ter
|
|
XM_011510784.2:c.3254C>A
|
XP_011509086.1:p.Ser1085Ter
|
|
XM_011510785.3:c.3239C>A
|
XP_011509087.1:p.Ser1080Ter
|
|
XM_011510786.3:c.3134C>A
|
XP_011509088.1:p.Ser1045Ter
|
|
XM_011510789.2:c.2948C>A
|
XP_011509091.1:p.Ser983Ter
|
|
XM_011510792.3:c.3425C>A
|
XP_011509094.1:p.Ser1142Ter
|
|
XM_017003568.1:c.3371C>A
|
XP_016859057.1:p.Ser1124Ter
|
|
XM_017003569.1:c.3203C>A
|
XP_016859058.1:p.Ser1068Ter
|
|
XM_017003570.1:c.2930C>A
|
XP_016859059.1:p.Ser977Ter
|
|
XM_017003571.1:c.2780C>A
|
XP_016859060.1:p.Ser927Ter
|
|
XM_017003572.1:c.2432C>A
|
XP_016859061.1:p.Ser811Ter
|
|
XM_017003573.1:c.2432C>A
|
XP_016859062.1:p.Ser811Ter
|
|
XM_017003574.1:c.2432C>A
|
XP_016859063.1:p.Ser811Ter
|
|
NM_015040.4:c.3389C>A
MANE Select
|
NP_055855.2:p.Ser1130Ter
|
|