ENST00000642496.1:c.3932G>C
|
|
|
ENST00000644397.2:c.5073G>C
MANE Select
|
ENSP00000495195.1:p.Arg1691Ser
|
|
ENST00000373965.6:c.4884G>C
|
ENSP00000363076.3:p.Arg1628Ser
|
|
ENST00000414778.5:c.4881G>C
|
ENSP00000410304.2:p.Arg1627Ser
|
|
ENST00000495484.5:c.1101G>C
|
ENSP00000480780.1:p.Arg367Ser
|
|
ENST00000614895.4:c.4896G>C
|
ENSP00000478512.1:p.Arg1632Ser
|
|
ENST00000616114.4:c.4878G>C
|
ENSP00000483745.1:p.Arg1626Ser
|
|
ENST00000618301.4:c.1233G>C
|
ENSP00000482780.1:p.Arg411Ser
|
|
ENST00000621708.4:c.4899G>C
|
ENSP00000484454.1:p.Arg1633Ser
|
|
NM_001142771.1:c.4899G>C
|
NP_001136243.1:p.Arg1633Ser
|
|
NM_001142772.1:c.4884G>C
|
NP_001136244.1:p.Arg1628Ser
|
|
NM_001354420.1:c.4878G>C
|
NP_001341349.1:p.Arg1626Ser
|
|
NM_001354429.1:c.5007G>C
|
NP_001341358.1:p.Arg1669Ser
|
|
XR_001747192.2:n.11365G>C
|
|
|
XR_001747193.2:n.11356G>C
|
|
|
NM_001142771.2:c.4899G>C
|
NP_001136243.1:p.Arg1633Ser
|
|
NM_001142772.2:c.4884G>C
|
NP_001136244.1:p.Arg1628Ser
|
|
NM_001354420.2:c.4878G>C
|
NP_001341349.1:p.Arg1626Ser
|
|
NM_001354429.2:c.5007G>C
|
NP_001341358.1:p.Arg1669Ser
|
|
NM_001384140.1:c.5073G>C
MANE Select
|
NP_001371069.1:p.Arg1691Ser
|
|