ENST00000642683.1:c.714G>T
|
ENSP00000495376.1:p.Trp238Cys
|
|
ENST00000643672.1:c.711G>T
|
ENSP00000494532.1:p.Trp237Cys
|
|
ENST00000645280.1:c.708G>T
|
ENSP00000496690.1:p.Trp236Cys
|
|
ENST00000648579.1:c.*59G>T
|
ENSP00000497638.1:n.*59G>T
|
|
ENST00000650617.1:c.762G>T
MANE Select
|
ENSP00000497532.1:p.Trp254Cys
|
|
ENST00000273158.8:c.762G>T
|
ENSP00000273158.3:p.Trp254Cys
|
|
NM_017875.2:c.762G>T
|
NP_060345.2:p.Trp254Cys
|
|
XM_006713214.1:c.750G>T
|
XP_006713277.1:p.Trp250Cys
|
|
XM_011533869.1:c.744G>T
|
XP_011532171.1:p.Trp248Cys
|
|
XM_011533870.1:c.711G>T
|
XP_011532172.1:p.Trp237Cys
|
|
XM_011533871.1:c.582G>T
|
XP_011532173.1:p.Trp194Cys
|
|
NM_001354798.1:c.626-1852G>T
|
NP_001341727.1:n.626-1852G>T
|
|
NM_017875.4:c.762G>T
MANE Select
|
NP_060345.2:p.Trp254Cys
|
|
XM_006713214.2:c.750G>T
|
XP_006713277.1:p.Trp250Cys
|
|
XM_011533869.2:c.744G>T
|
XP_011532171.1:p.Trp248Cys
|
|
XM_024453611.1:c.708G>T
|
XP_024309379.1:p.Trp236Cys
|
|
NM_001354798.2:c.626-1852G>T
|
NP_001341727.1:n.626-1852G>T
|
|