ENST00000264380.9:c.3460G>T
MANE Select
|
ENSP00000264380.4:p.Asp1154Tyr
|
|
ENST00000264380.8:c.3460G>T
|
ENSP00000264380.4:p.Asp1154Tyr
|
|
ENST00000452564.1:c.3292G>T
|
ENSP00000405736.1:p.Asp1098Tyr
|
|
NM_015040.3:c.3460G>T
|
NP_055855.2:p.Asp1154Tyr
|
|
XM_011510778.1:c.3496G>T
|
XP_011509080.1:p.Asp1166Tyr
|
|
XM_011510779.1:c.3496G>T
|
XP_011509081.1:p.Asp1166Tyr
|
|
XM_011510780.1:c.3493G>T
|
XP_011509082.1:p.Asp1165Tyr
|
|
XM_011510781.1:c.3478G>T
|
XP_011509083.1:p.Asp1160Tyr
|
|
XM_011510782.1:c.3496G>T
|
XP_011509084.1:p.Asp1166Tyr
|
|
XM_011510783.1:c.3328G>T
|
XP_011509085.1:p.Asp1110Tyr
|
|
XM_011510784.1:c.3325G>T
|
XP_011509086.1:p.Asp1109Tyr
|
|
XM_011510785.1:c.3310G>T
|
XP_011509087.1:p.Asp1104Tyr
|
|
XM_011510786.1:c.3205G>T
|
XP_011509088.1:p.Asp1069Tyr
|
|
XM_011510787.1:c.3202G>T
|
XP_011509089.1:p.Asp1068Tyr
|
|
XM_011510788.1:c.3169G>T
|
XP_011509090.1:p.Asp1057Tyr
|
|
XM_011510789.1:c.3019G>T
|
XP_011509091.1:p.Asp1007Tyr
|
|
XM_011510790.1:c.2503G>T
|
XP_011509092.1:p.Asp835Tyr
|
|
XM_011510791.1:c.2503G>T
|
XP_011509093.1:p.Asp835Tyr
|
|
XM_011510792.1:c.3496G>T
|
XP_011509094.1:p.Asp1166Tyr
|
|
XR_922888.1:n.3633G>T
|
|
|
XM_011510778.3:c.3496G>T
|
XP_011509080.1:p.Asp1166Tyr
|
|
XM_011510779.2:c.3496G>T
|
XP_011509081.1:p.Asp1166Tyr
|
|
XM_011510780.2:c.3493G>T
|
XP_011509082.1:p.Asp1165Tyr
|
|
XM_011510781.3:c.3478G>T
|
XP_011509083.1:p.Asp1160Tyr
|
|
XM_011510782.3:c.3496G>T
|
XP_011509084.1:p.Asp1166Tyr
|
|
XM_011510783.3:c.3328G>T
|
XP_011509085.1:p.Asp1110Tyr
|
|
XM_011510784.2:c.3325G>T
|
XP_011509086.1:p.Asp1109Tyr
|
|
XM_011510785.3:c.3310G>T
|
XP_011509087.1:p.Asp1104Tyr
|
|
XM_011510786.3:c.3205G>T
|
XP_011509088.1:p.Asp1069Tyr
|
|
XM_011510789.2:c.3019G>T
|
XP_011509091.1:p.Asp1007Tyr
|
|
XM_011510792.3:c.3496G>T
|
XP_011509094.1:p.Asp1166Tyr
|
|
XM_017003568.1:c.3442G>T
|
XP_016859057.1:p.Asp1148Tyr
|
|
XM_017003569.1:c.3274G>T
|
XP_016859058.1:p.Asp1092Tyr
|
|
XM_017003570.1:c.3001G>T
|
XP_016859059.1:p.Asp1001Tyr
|
|
XM_017003571.1:c.2851G>T
|
XP_016859060.1:p.Asp951Tyr
|
|
XM_017003572.1:c.2503G>T
|
XP_016859061.1:p.Asp835Tyr
|
|
XM_017003573.1:c.2503G>T
|
XP_016859062.1:p.Asp835Tyr
|
|
XM_017003574.1:c.2503G>T
|
XP_016859063.1:p.Asp835Tyr
|
|
NM_015040.4:c.3460G>T
MANE Select
|
NP_055855.2:p.Asp1154Tyr
|
|