ENST00000248633.9:c.1983G>T
MANE Select
|
ENSP00000248633.4:p.Leu661=
|
|
ENST00000248633.8:c.1983G>T
|
ENSP00000248633.4:p.Leu661=
|
|
ENST00000428214.5:c.1900+1428G>T
|
ENSP00000394413.1:n.1900+1428G>T
|
|
ENST00000438045.5:c.1017G>T
|
ENSP00000410438.1:p.Leu339=
|
|
ENST00000484913.5:n.2022G>T
|
|
|
ENST00000496420.5:n.1659G>T
|
|
|
NM_000466.2:c.1983G>T
|
NP_000457.1:p.Leu661=
|
|
NM_001282677.1:c.1900+1428G>T
|
NP_001269606.1:n.1900+1428G>T
|
|
NM_001282678.1:c.1359G>T
|
NP_001269607.1:p.Leu453=
|
|
XM_005250433.3:c.234G>T
|
XP_005250490.1:p.Leu78=
|
|
XR_242246.3:n.2079G>T
|
|
|
XM_017012319.2:c.234G>T
|
XP_016867808.1:p.Leu78=
|
|
XR_001744808.2:n.1010G>T
|
|
|
XR_242246.5:n.2030G>T
|
|
|
NM_000466.3:c.1983G>T
MANE Select
|
NP_000457.1:p.Leu661=
|
|
NM_001282677.2:c.1900+1428G>T
|
NP_001269606.1:n.1900+1428G>T
|
|
NM_001282678.2:c.1359G>T
|
NP_001269607.1:p.Leu453=
|
|