ENST00000248633.9:c.2387T>G
MANE Select
|
ENSP00000248633.4:p.Leu796Arg
|
|
ENST00000248633.8:c.2387T>G
|
ENSP00000248633.4:p.Leu796Arg
|
|
ENST00000428214.5:c.2216T>G
|
ENSP00000394413.1:p.Leu739Arg
|
|
ENST00000438045.5:c.1421T>G
|
ENSP00000410438.1:p.Leu474Arg
|
|
ENST00000484913.5:n.2426T>G
|
|
|
ENST00000496092.1:n.185T>G
|
|
|
ENST00000496420.5:n.2063T>G
|
|
|
NM_000466.2:c.2387T>G
|
NP_000457.1:p.Leu796Arg
|
|
NM_001282677.1:c.2216T>G
|
NP_001269606.1:p.Leu739Arg
|
|
NM_001282678.1:c.1763T>G
|
NP_001269607.1:p.Leu588Arg
|
|
XM_005250433.3:c.638T>G
|
XP_005250490.1:p.Leu213Arg
|
|
XR_242246.3:n.2483T>G
|
|
|
XM_017012319.2:c.638T>G
|
XP_016867808.1:p.Leu213Arg
|
|
XR_001744808.2:n.1414T>G
|
|
|
XR_242246.5:n.2434T>G
|
|
|
NM_000466.3:c.2387T>G
MANE Select
|
NP_000457.1:p.Leu796Arg
|
|
NM_001282677.2:c.2216T>G
|
NP_001269606.1:p.Leu739Arg
|
|
NM_001282678.2:c.1763T>G
|
NP_001269607.1:p.Leu588Arg
|
|