ENST00000248633.9:c.1824A>G
MANE Select
|
ENSP00000248633.4:p.Leu608=
|
|
ENST00000248633.8:c.1824A>G
|
ENSP00000248633.4:p.Leu608=
|
|
ENST00000422866.1:c.642A>G
|
|
|
ENST00000428214.5:c.1824A>G
|
ENSP00000394413.1:p.Leu608=
|
|
ENST00000438045.5:c.858A>G
|
ENSP00000410438.1:p.Leu286=
|
|
ENST00000484913.5:n.1863A>G
|
|
|
ENST00000496420.5:n.1500A>G
|
|
|
NM_000466.2:c.1824A>G
|
NP_000457.1:p.Leu608=
|
|
NM_001282677.1:c.1824A>G
|
NP_001269606.1:p.Leu608=
|
|
NM_001282678.1:c.1200A>G
|
NP_001269607.1:p.Leu400=
|
|
XM_005250433.3:c.75A>G
|
XP_005250490.1:p.Leu25=
|
|
XR_242246.3:n.1920A>G
|
|
|
XM_017012319.2:c.75A>G
|
XP_016867808.1:p.Leu25=
|
|
XR_001744808.2:n.851A>G
|
|
|
XR_242246.5:n.1871A>G
|
|
|
NM_000466.3:c.1824A>G
MANE Select
|
NP_000457.1:p.Leu608=
|
|
NM_001282677.2:c.1824A>G
|
NP_001269606.1:p.Leu608=
|
|
NM_001282678.2:c.1200A>G
|
NP_001269607.1:p.Leu400=
|
|