ENST00000248633.9:c.1911T>G
MANE Select
|
ENSP00000248633.4:p.Leu637=
|
|
ENST00000248633.8:c.1911T>G
|
ENSP00000248633.4:p.Leu637=
|
|
ENST00000422866.1:c.729T>G
|
|
|
ENST00000428214.5:c.1900+1356T>G
|
ENSP00000394413.1:n.1900+1356T>G
|
|
ENST00000438045.5:c.945T>G
|
ENSP00000410438.1:p.Leu315=
|
|
ENST00000484913.5:n.1950T>G
|
|
|
ENST00000496420.5:n.1587T>G
|
|
|
NM_000466.2:c.1911T>G
|
NP_000457.1:p.Leu637=
|
|
NM_001282677.1:c.1900+1356T>G
|
NP_001269606.1:n.1900+1356T>G
|
|
NM_001282678.1:c.1287T>G
|
NP_001269607.1:p.Leu429=
|
|
XM_005250433.3:c.162T>G
|
XP_005250490.1:p.Leu54=
|
|
XR_242246.3:n.2007T>G
|
|
|
XM_017012319.2:c.162T>G
|
XP_016867808.1:p.Leu54=
|
|
XR_001744808.2:n.938T>G
|
|
|
XR_242246.5:n.1958T>G
|
|
|
NM_000466.3:c.1911T>G
MANE Select
|
NP_000457.1:p.Leu637=
|
|
NM_001282677.2:c.1900+1356T>G
|
NP_001269606.1:n.1900+1356T>G
|
|
NM_001282678.2:c.1287T>G
|
NP_001269607.1:p.Leu429=
|
|