ENST00000248633.9:c.2695A>T
MANE Select
|
ENSP00000248633.4:p.Arg899Ter
|
|
ENST00000248633.8:c.2695A>T
|
ENSP00000248633.4:p.Arg899Ter
|
|
ENST00000428214.5:c.2524A>T
|
ENSP00000394413.1:p.Arg842Ter
|
|
ENST00000438045.5:c.1729A>T
|
ENSP00000410438.1:p.Arg577Ter
|
|
ENST00000484913.5:n.2734A>T
|
|
|
ENST00000496420.5:n.2587A>T
|
|
|
NM_000466.2:c.2695A>T
|
NP_000457.1:p.Arg899Ter
|
|
NM_001282677.1:c.2524A>T
|
NP_001269606.1:p.Arg842Ter
|
|
NM_001282678.1:c.2071A>T
|
NP_001269607.1:p.Arg691Ter
|
|
XM_005250433.3:c.946A>T
|
XP_005250490.1:p.Arg316Ter
|
|
XR_242246.3:n.2791A>T
|
|
|
XM_017012319.2:c.946A>T
|
XP_016867808.1:p.Arg316Ter
|
|
XR_001744808.2:n.1722A>T
|
|
|
XR_242246.5:n.2742A>T
|
|
|
NM_000466.3:c.2695A>T
MANE Select
|
NP_000457.1:p.Arg899Ter
|
|
NM_001282677.2:c.2524A>T
|
NP_001269606.1:p.Arg842Ter
|
|
NM_001282678.2:c.2071A>T
|
NP_001269607.1:p.Arg691Ter
|
|