ENST00000642496.1:c.4035T>C
|
|
|
ENST00000644397.2:c.5176T>C
MANE Select
|
ENSP00000495195.1:p.Trp1726Arg
|
|
ENST00000373965.6:c.4987T>C
|
ENSP00000363076.3:p.Trp1663Arg
|
|
ENST00000414778.5:c.4984T>C
|
ENSP00000410304.2:p.Trp1662Arg
|
|
ENST00000495484.5:c.1204T>C
|
ENSP00000480780.1:p.Trp402Arg
|
|
ENST00000614895.4:c.4999T>C
|
ENSP00000478512.1:p.Trp1667Arg
|
|
ENST00000616114.4:c.4981T>C
|
ENSP00000483745.1:p.Trp1661Arg
|
|
ENST00000618301.4:c.1336T>C
|
ENSP00000482780.1:p.Trp446Arg
|
|
ENST00000621708.4:c.5002T>C
|
ENSP00000484454.1:p.Trp1668Arg
|
|
NM_001142771.1:c.5002T>C
|
NP_001136243.1:p.Trp1668Arg
|
|
NM_001142772.1:c.4987T>C
|
NP_001136244.1:p.Trp1663Arg
|
|
NM_001354420.1:c.4981T>C
|
NP_001341349.1:p.Trp1661Arg
|
|
NM_001354429.1:c.5110T>C
|
NP_001341358.1:p.Trp1704Arg
|
|
XR_001747192.2:n.11468T>C
|
|
|
XR_001747193.2:n.11459T>C
|
|
|
NM_001142771.2:c.5002T>C
|
NP_001136243.1:p.Trp1668Arg
|
|
NM_001142772.2:c.4987T>C
|
NP_001136244.1:p.Trp1663Arg
|
|
NM_001354420.2:c.4981T>C
|
NP_001341349.1:p.Trp1661Arg
|
|
NM_001354429.2:c.5110T>C
|
NP_001341358.1:p.Trp1704Arg
|
|
NM_001384140.1:c.5176T>C
MANE Select
|
NP_001371069.1:p.Trp1726Arg
|
|