ENST00000248633.9:c.2274C>T
MANE Select
|
ENSP00000248633.4:p.Asp758=
|
|
ENST00000248633.8:c.2274C>T
|
ENSP00000248633.4:p.Asp758=
|
|
ENST00000428214.5:c.2103C>T
|
ENSP00000394413.1:p.Asp701=
|
|
ENST00000438045.5:c.1308C>T
|
ENSP00000410438.1:p.Asp436=
|
|
ENST00000484913.5:n.2313C>T
|
|
|
ENST00000496092.1:n.72C>T
|
|
|
ENST00000496420.5:n.1950C>T
|
|
|
NM_000466.2:c.2274C>T
|
NP_000457.1:p.Asp758=
|
|
NM_001282677.1:c.2103C>T
|
NP_001269606.1:p.Asp701=
|
|
NM_001282678.1:c.1650C>T
|
NP_001269607.1:p.Asp550=
|
|
XM_005250433.3:c.525C>T
|
XP_005250490.1:p.Asp175=
|
|
XR_242246.3:n.2370C>T
|
|
|
XM_017012319.2:c.525C>T
|
XP_016867808.1:p.Asp175=
|
|
XR_001744808.2:n.1301C>T
|
|
|
XR_242246.5:n.2321C>T
|
|
|
NM_000466.3:c.2274C>T
MANE Select
|
NP_000457.1:p.Asp758=
|
|
NM_001282677.2:c.2103C>T
|
NP_001269606.1:p.Asp701=
|
|
NM_001282678.2:c.1650C>T
|
NP_001269607.1:p.Asp550=
|
|