ENST00000264380.9:c.3405C>G
MANE Select
|
ENSP00000264380.4:p.Ser1135Arg
|
|
ENST00000264380.8:c.3405C>G
|
ENSP00000264380.4:p.Ser1135Arg
|
|
ENST00000452564.1:c.3237C>G
|
ENSP00000405736.1:p.Ser1079Arg
|
|
NM_015040.3:c.3405C>G
|
NP_055855.2:p.Ser1135Arg
|
|
XM_011510778.1:c.3441C>G
|
XP_011509080.1:p.Ser1147Arg
|
|
XM_011510779.1:c.3441C>G
|
XP_011509081.1:p.Ser1147Arg
|
|
XM_011510780.1:c.3438C>G
|
XP_011509082.1:p.Ser1146Arg
|
|
XM_011510781.1:c.3423C>G
|
XP_011509083.1:p.Ser1141Arg
|
|
XM_011510782.1:c.3441C>G
|
XP_011509084.1:p.Ser1147Arg
|
|
XM_011510783.1:c.3273C>G
|
XP_011509085.1:p.Ser1091Arg
|
|
XM_011510784.1:c.3270C>G
|
XP_011509086.1:p.Ser1090Arg
|
|
XM_011510785.1:c.3255C>G
|
XP_011509087.1:p.Ser1085Arg
|
|
XM_011510786.1:c.3150C>G
|
XP_011509088.1:p.Ser1050Arg
|
|
XM_011510787.1:c.3147C>G
|
XP_011509089.1:p.Ser1049Arg
|
|
XM_011510788.1:c.3114C>G
|
XP_011509090.1:p.Ser1038Arg
|
|
XM_011510789.1:c.2964C>G
|
XP_011509091.1:p.Ser988Arg
|
|
XM_011510790.1:c.2448C>G
|
XP_011509092.1:p.Ser816Arg
|
|
XM_011510791.1:c.2448C>G
|
XP_011509093.1:p.Ser816Arg
|
|
XM_011510792.1:c.3441C>G
|
XP_011509094.1:p.Ser1147Arg
|
|
XR_922888.1:n.3578C>G
|
|
|
XM_011510778.3:c.3441C>G
|
XP_011509080.1:p.Ser1147Arg
|
|
XM_011510779.2:c.3441C>G
|
XP_011509081.1:p.Ser1147Arg
|
|
XM_011510780.2:c.3438C>G
|
XP_011509082.1:p.Ser1146Arg
|
|
XM_011510781.3:c.3423C>G
|
XP_011509083.1:p.Ser1141Arg
|
|
XM_011510782.3:c.3441C>G
|
XP_011509084.1:p.Ser1147Arg
|
|
XM_011510783.3:c.3273C>G
|
XP_011509085.1:p.Ser1091Arg
|
|
XM_011510784.2:c.3270C>G
|
XP_011509086.1:p.Ser1090Arg
|
|
XM_011510785.3:c.3255C>G
|
XP_011509087.1:p.Ser1085Arg
|
|
XM_011510786.3:c.3150C>G
|
XP_011509088.1:p.Ser1050Arg
|
|
XM_011510789.2:c.2964C>G
|
XP_011509091.1:p.Ser988Arg
|
|
XM_011510792.3:c.3441C>G
|
XP_011509094.1:p.Ser1147Arg
|
|
XM_017003568.1:c.3387C>G
|
XP_016859057.1:p.Ser1129Arg
|
|
XM_017003569.1:c.3219C>G
|
XP_016859058.1:p.Ser1073Arg
|
|
XM_017003570.1:c.2946C>G
|
XP_016859059.1:p.Ser982Arg
|
|
XM_017003571.1:c.2796C>G
|
XP_016859060.1:p.Ser932Arg
|
|
XM_017003572.1:c.2448C>G
|
XP_016859061.1:p.Ser816Arg
|
|
XM_017003573.1:c.2448C>G
|
XP_016859062.1:p.Ser816Arg
|
|
XM_017003574.1:c.2448C>G
|
XP_016859063.1:p.Ser816Arg
|
|
NM_015040.4:c.3405C>G
MANE Select
|
NP_055855.2:p.Ser1135Arg
|
|