ENST00000642496.1:c.3887C>T
|
|
|
ENST00000644397.2:c.5028C>T
MANE Select
|
ENSP00000495195.1:p.Cys1676=
|
|
ENST00000373965.6:c.4839C>T
|
ENSP00000363076.3:p.Cys1613=
|
|
ENST00000414778.5:c.4836C>T
|
ENSP00000410304.2:p.Cys1612=
|
|
ENST00000495484.5:c.1056C>T
|
ENSP00000480780.1:p.Cys352=
|
|
ENST00000614895.4:c.4851C>T
|
ENSP00000478512.1:p.Cys1617=
|
|
ENST00000616114.4:c.4833C>T
|
ENSP00000483745.1:p.Cys1611=
|
|
ENST00000618301.4:c.1188C>T
|
ENSP00000482780.1:p.Cys396=
|
|
ENST00000621708.4:c.4854C>T
|
ENSP00000484454.1:p.Cys1618=
|
|
NM_001142771.1:c.4854C>T
|
NP_001136243.1:p.Cys1618=
|
|
NM_001142772.1:c.4839C>T
|
NP_001136244.1:p.Cys1613=
|
|
NM_001354420.1:c.4833C>T
|
NP_001341349.1:p.Cys1611=
|
|
NM_001354429.1:c.4962C>T
|
NP_001341358.1:p.Cys1654=
|
|
XR_001747192.2:n.11320C>T
|
|
|
XR_001747193.2:n.11311C>T
|
|
|
NM_001142771.2:c.4854C>T
|
NP_001136243.1:p.Cys1618=
|
|
NM_001142772.2:c.4839C>T
|
NP_001136244.1:p.Cys1613=
|
|
NM_001354420.2:c.4833C>T
|
NP_001341349.1:p.Cys1611=
|
|
NM_001354429.2:c.4962C>T
|
NP_001341358.1:p.Cys1654=
|
|
NM_001384140.1:c.5028C>T
MANE Select
|
NP_001371069.1:p.Cys1676=
|
|