ENST00000264380.9:c.3497A>C
MANE Select
|
ENSP00000264380.4:p.Asn1166Thr
|
|
ENST00000264380.8:c.3497A>C
|
ENSP00000264380.4:p.Asn1166Thr
|
|
ENST00000452564.1:c.3329A>C
|
ENSP00000405736.1:p.Asn1110Thr
|
|
NM_015040.3:c.3497A>C
|
NP_055855.2:p.Asn1166Thr
|
|
XM_011510778.1:c.3533A>C
|
XP_011509080.1:p.Asn1178Thr
|
|
XM_011510779.1:c.3533A>C
|
XP_011509081.1:p.Asn1178Thr
|
|
XM_011510780.1:c.3530A>C
|
XP_011509082.1:p.Asn1177Thr
|
|
XM_011510781.1:c.3515A>C
|
XP_011509083.1:p.Asn1172Thr
|
|
XM_011510782.1:c.3533A>C
|
XP_011509084.1:p.Asn1178Thr
|
|
XM_011510783.1:c.3365A>C
|
XP_011509085.1:p.Asn1122Thr
|
|
XM_011510784.1:c.3362A>C
|
XP_011509086.1:p.Asn1121Thr
|
|
XM_011510785.1:c.3347A>C
|
XP_011509087.1:p.Asn1116Thr
|
|
XM_011510786.1:c.3242A>C
|
XP_011509088.1:p.Asn1081Thr
|
|
XM_011510787.1:c.3239A>C
|
XP_011509089.1:p.Asn1080Thr
|
|
XM_011510788.1:c.3206A>C
|
XP_011509090.1:p.Asn1069Thr
|
|
XM_011510789.1:c.3056A>C
|
XP_011509091.1:p.Asn1019Thr
|
|
XM_011510790.1:c.2540A>C
|
XP_011509092.1:p.Asn847Thr
|
|
XM_011510791.1:c.2540A>C
|
XP_011509093.1:p.Asn847Thr
|
|
XM_011510792.1:c.3533A>C
|
XP_011509094.1:p.Asn1178Thr
|
|
XR_922888.1:n.3670A>C
|
|
|
XM_011510778.3:c.3533A>C
|
XP_011509080.1:p.Asn1178Thr
|
|
XM_011510779.2:c.3533A>C
|
XP_011509081.1:p.Asn1178Thr
|
|
XM_011510780.2:c.3530A>C
|
XP_011509082.1:p.Asn1177Thr
|
|
XM_011510781.3:c.3515A>C
|
XP_011509083.1:p.Asn1172Thr
|
|
XM_011510782.3:c.3533A>C
|
XP_011509084.1:p.Asn1178Thr
|
|
XM_011510783.3:c.3365A>C
|
XP_011509085.1:p.Asn1122Thr
|
|
XM_011510784.2:c.3362A>C
|
XP_011509086.1:p.Asn1121Thr
|
|
XM_011510785.3:c.3347A>C
|
XP_011509087.1:p.Asn1116Thr
|
|
XM_011510786.3:c.3242A>C
|
XP_011509088.1:p.Asn1081Thr
|
|
XM_011510789.2:c.3056A>C
|
XP_011509091.1:p.Asn1019Thr
|
|
XM_011510792.3:c.3533A>C
|
XP_011509094.1:p.Asn1178Thr
|
|
XM_017003568.1:c.3479A>C
|
XP_016859057.1:p.Asn1160Thr
|
|
XM_017003569.1:c.3311A>C
|
XP_016859058.1:p.Asn1104Thr
|
|
XM_017003570.1:c.3038A>C
|
XP_016859059.1:p.Asn1013Thr
|
|
XM_017003571.1:c.2888A>C
|
XP_016859060.1:p.Asn963Thr
|
|
XM_017003572.1:c.2540A>C
|
XP_016859061.1:p.Asn847Thr
|
|
XM_017003573.1:c.2540A>C
|
XP_016859062.1:p.Asn847Thr
|
|
XM_017003574.1:c.2540A>C
|
XP_016859063.1:p.Asn847Thr
|
|
NM_015040.4:c.3497A>C
MANE Select
|
NP_055855.2:p.Asn1166Thr
|
|