ENST00000255078.8:c.1818C>T
MANE Select
|
ENSP00000255078.4:p.Arg606=
|
|
ENST00000674675.1:c.62C>T
|
|
|
ENST00000674878.1:c.62C>T
|
|
|
ENST00000674955.1:c.*535C>T
|
ENSP00000502463.1:n.*535C>T
|
|
ENST00000675118.1:c.1306C>T
|
|
|
ENST00000675389.1:n.93C>T
|
|
|
ENST00000675615.1:c.1818C>T
|
ENSP00000502413.1:p.Arg606=
|
|
ENST00000675648.1:n.1193C>T
|
|
|
ENST00000675916.1:c.62C>T
|
|
|
ENST00000676173.1:n.2563C>T
|
|
|
ENST00000676182.1:c.249C>T
|
|
|
ENST00000676228.1:c.*1141C>T
|
ENSP00000502375.1:n.*1141C>T
|
|
ENST00000255078.7:c.1818C>T
|
ENSP00000255078.3:p.Arg606=
|
|
ENST00000539064.5:n.1577C>T
|
|
|
ENST00000541229.5:n.513C>T
|
|
|
ENST00000543739.5:n.811C>T
|
|
|
ENST00000545475.1:n.414C>T
|
|
|
NM_002180.2:c.1818C>T , LRG_250t1:c.1818C>T
|
NP_002171.2:p.Arg606=
|
|
XM_005273974.2:c.807C>T
|
XP_005274031.1:p.Arg269=
|
|
XM_005273975.2:c.690C>T
|
XP_005274032.1:p.Arg230=
|
|
XM_011544994.1:c.585C>T
|
XP_011543296.1:p.Arg195=
|
|
XR_949903.1:n.1920C>T
|
|
|
XM_005273975.3:c.690C>T
|
XP_005274032.1:p.Arg230=
|
|
XM_017017669.2:c.807C>T
|
XP_016873158.1:p.Arg269=
|
|
XM_017017670.2:c.807C>T
|
XP_016873159.1:p.Arg269=
|
|
XR_949903.3:n.1916C>T
|
|
|
NM_002180.3:c.1818C>T
MANE Select
|
NP_002171.2:p.Arg606=
|
|