ENST00000264414.9:c.1260G>C
MANE Select
|
ENSP00000264414.4:p.Arg420Ser
|
|
ENST00000264414.8:c.1260G>C
|
ENSP00000264414.4:p.Arg420Ser
|
|
ENST00000344951.8:c.1062G>C
|
ENSP00000343601.4:p.Arg354Ser
|
|
ENST00000409096.5:c.1188G>C
|
ENSP00000387200.1:p.Arg396Ser
|
|
ENST00000409777.5:c.1188G>C
|
ENSP00000386525.1:p.Arg396Ser
|
|
ENST00000481135.1:n.556G>C
|
|
|
ENST00000617432.4:c.-17G>C
|
ENSP00000477851.1:n.-17G>C
|
|
NM_001257197.1:c.1062G>C
|
NP_001244126.1:p.Arg354Ser
|
|
NM_001257198.1:c.1278G>C
|
NP_001244127.1:p.Arg426Ser
|
|
NM_003590.4:c.1260G>C
|
NP_003581.1:p.Arg420Ser
|
|
XM_006712800.2:c.1227G>C
|
XP_006712863.2:p.Arg409Ser
|
|
XM_011511994.1:c.1113G>C
|
XP_011510296.1:p.Arg371Ser
|
|
XM_011511995.1:c.1218G>C
|
XP_011510297.1:p.Arg406Ser
|
|
XM_011511996.1:c.1068G>C
|
XP_011510298.1:p.Arg356Ser
|
|
XM_011511997.1:c.960G>C
|
XP_011510299.1:p.Arg320Ser
|
|
XM_011511994.3:c.1113G>C
|
XP_011510296.1:p.Arg371Ser
|
|
XM_011511996.2:c.1068G>C
|
XP_011510298.1:p.Arg356Ser
|
|
NM_003590.5:c.1260G>C
MANE Select
|
NP_003581.1:p.Arg420Ser
|
|
NM_001257198.2:c.1278G>C
|
NP_001244127.1:p.Arg426Ser
|
|
NM_001257197.2:c.1062G>C
|
NP_001244126.1:p.Arg354Ser
|
|