ENST00000264380.9:c.3483A>C
MANE Select
|
ENSP00000264380.4:p.Arg1161Ser
|
|
ENST00000264380.8:c.3483A>C
|
ENSP00000264380.4:p.Arg1161Ser
|
|
ENST00000452564.1:c.3315A>C
|
ENSP00000405736.1:p.Arg1105Ser
|
|
NM_015040.3:c.3483A>C
|
NP_055855.2:p.Arg1161Ser
|
|
XM_011510778.1:c.3519A>C
|
XP_011509080.1:p.Arg1173Ser
|
|
XM_011510779.1:c.3519A>C
|
XP_011509081.1:p.Arg1173Ser
|
|
XM_011510780.1:c.3516A>C
|
XP_011509082.1:p.Arg1172Ser
|
|
XM_011510781.1:c.3501A>C
|
XP_011509083.1:p.Arg1167Ser
|
|
XM_011510782.1:c.3519A>C
|
XP_011509084.1:p.Arg1173Ser
|
|
XM_011510783.1:c.3351A>C
|
XP_011509085.1:p.Arg1117Ser
|
|
XM_011510784.1:c.3348A>C
|
XP_011509086.1:p.Arg1116Ser
|
|
XM_011510785.1:c.3333A>C
|
XP_011509087.1:p.Arg1111Ser
|
|
XM_011510786.1:c.3228A>C
|
XP_011509088.1:p.Arg1076Ser
|
|
XM_011510787.1:c.3225A>C
|
XP_011509089.1:p.Arg1075Ser
|
|
XM_011510788.1:c.3192A>C
|
XP_011509090.1:p.Arg1064Ser
|
|
XM_011510789.1:c.3042A>C
|
XP_011509091.1:p.Arg1014Ser
|
|
XM_011510790.1:c.2526A>C
|
XP_011509092.1:p.Arg842Ser
|
|
XM_011510791.1:c.2526A>C
|
XP_011509093.1:p.Arg842Ser
|
|
XM_011510792.1:c.3519A>C
|
XP_011509094.1:p.Arg1173Ser
|
|
XR_922888.1:n.3656A>C
|
|
|
XM_011510778.3:c.3519A>C
|
XP_011509080.1:p.Arg1173Ser
|
|
XM_011510779.2:c.3519A>C
|
XP_011509081.1:p.Arg1173Ser
|
|
XM_011510780.2:c.3516A>C
|
XP_011509082.1:p.Arg1172Ser
|
|
XM_011510781.3:c.3501A>C
|
XP_011509083.1:p.Arg1167Ser
|
|
XM_011510782.3:c.3519A>C
|
XP_011509084.1:p.Arg1173Ser
|
|
XM_011510783.3:c.3351A>C
|
XP_011509085.1:p.Arg1117Ser
|
|
XM_011510784.2:c.3348A>C
|
XP_011509086.1:p.Arg1116Ser
|
|
XM_011510785.3:c.3333A>C
|
XP_011509087.1:p.Arg1111Ser
|
|
XM_011510786.3:c.3228A>C
|
XP_011509088.1:p.Arg1076Ser
|
|
XM_011510789.2:c.3042A>C
|
XP_011509091.1:p.Arg1014Ser
|
|
XM_011510792.3:c.3519A>C
|
XP_011509094.1:p.Arg1173Ser
|
|
XM_017003568.1:c.3465A>C
|
XP_016859057.1:p.Arg1155Ser
|
|
XM_017003569.1:c.3297A>C
|
XP_016859058.1:p.Arg1099Ser
|
|
XM_017003570.1:c.3024A>C
|
XP_016859059.1:p.Arg1008Ser
|
|
XM_017003571.1:c.2874A>C
|
XP_016859060.1:p.Arg958Ser
|
|
XM_017003572.1:c.2526A>C
|
XP_016859061.1:p.Arg842Ser
|
|
XM_017003573.1:c.2526A>C
|
XP_016859062.1:p.Arg842Ser
|
|
XM_017003574.1:c.2526A>C
|
XP_016859063.1:p.Arg842Ser
|
|
NM_015040.4:c.3483A>C
MANE Select
|
NP_055855.2:p.Arg1161Ser
|
|