ENST00000264380.9:c.3440G>A
MANE Select
|
ENSP00000264380.4:p.Ser1147Asn
|
|
ENST00000264380.8:c.3440G>A
|
ENSP00000264380.4:p.Ser1147Asn
|
|
ENST00000452564.1:c.3272G>A
|
ENSP00000405736.1:p.Ser1091Asn
|
|
NM_015040.3:c.3440G>A
|
NP_055855.2:p.Ser1147Asn
|
|
XM_011510778.1:c.3476G>A
|
XP_011509080.1:p.Ser1159Asn
|
|
XM_011510779.1:c.3476G>A
|
XP_011509081.1:p.Ser1159Asn
|
|
XM_011510780.1:c.3473G>A
|
XP_011509082.1:p.Ser1158Asn
|
|
XM_011510781.1:c.3458G>A
|
XP_011509083.1:p.Ser1153Asn
|
|
XM_011510782.1:c.3476G>A
|
XP_011509084.1:p.Ser1159Asn
|
|
XM_011510783.1:c.3308G>A
|
XP_011509085.1:p.Ser1103Asn
|
|
XM_011510784.1:c.3305G>A
|
XP_011509086.1:p.Ser1102Asn
|
|
XM_011510785.1:c.3290G>A
|
XP_011509087.1:p.Ser1097Asn
|
|
XM_011510786.1:c.3185G>A
|
XP_011509088.1:p.Ser1062Asn
|
|
XM_011510787.1:c.3182G>A
|
XP_011509089.1:p.Ser1061Asn
|
|
XM_011510788.1:c.3149G>A
|
XP_011509090.1:p.Ser1050Asn
|
|
XM_011510789.1:c.2999G>A
|
XP_011509091.1:p.Ser1000Asn
|
|
XM_011510790.1:c.2483G>A
|
XP_011509092.1:p.Ser828Asn
|
|
XM_011510791.1:c.2483G>A
|
XP_011509093.1:p.Ser828Asn
|
|
XM_011510792.1:c.3476G>A
|
XP_011509094.1:p.Ser1159Asn
|
|
XR_922888.1:n.3613G>A
|
|
|
XM_011510778.3:c.3476G>A
|
XP_011509080.1:p.Ser1159Asn
|
|
XM_011510779.2:c.3476G>A
|
XP_011509081.1:p.Ser1159Asn
|
|
XM_011510780.2:c.3473G>A
|
XP_011509082.1:p.Ser1158Asn
|
|
XM_011510781.3:c.3458G>A
|
XP_011509083.1:p.Ser1153Asn
|
|
XM_011510782.3:c.3476G>A
|
XP_011509084.1:p.Ser1159Asn
|
|
XM_011510783.3:c.3308G>A
|
XP_011509085.1:p.Ser1103Asn
|
|
XM_011510784.2:c.3305G>A
|
XP_011509086.1:p.Ser1102Asn
|
|
XM_011510785.3:c.3290G>A
|
XP_011509087.1:p.Ser1097Asn
|
|
XM_011510786.3:c.3185G>A
|
XP_011509088.1:p.Ser1062Asn
|
|
XM_011510789.2:c.2999G>A
|
XP_011509091.1:p.Ser1000Asn
|
|
XM_011510792.3:c.3476G>A
|
XP_011509094.1:p.Ser1159Asn
|
|
XM_017003568.1:c.3422G>A
|
XP_016859057.1:p.Ser1141Asn
|
|
XM_017003569.1:c.3254G>A
|
XP_016859058.1:p.Ser1085Asn
|
|
XM_017003570.1:c.2981G>A
|
XP_016859059.1:p.Ser994Asn
|
|
XM_017003571.1:c.2831G>A
|
XP_016859060.1:p.Ser944Asn
|
|
XM_017003572.1:c.2483G>A
|
XP_016859061.1:p.Ser828Asn
|
|
XM_017003573.1:c.2483G>A
|
XP_016859062.1:p.Ser828Asn
|
|
XM_017003574.1:c.2483G>A
|
XP_016859063.1:p.Ser828Asn
|
|
NM_015040.4:c.3440G>A
MANE Select
|
NP_055855.2:p.Ser1147Asn
|
|