ENST00000248633.9:c.1508T>G
MANE Select
|
ENSP00000248633.4:p.Ile503Arg
|
|
ENST00000248633.8:c.1508T>G
|
ENSP00000248633.4:p.Ile503Arg
|
|
ENST00000422866.1:c.409T>G
|
|
|
ENST00000428214.5:c.1508T>G
|
ENSP00000394413.1:p.Ile503Arg
|
|
ENST00000438045.5:c.542T>G
|
ENSP00000410438.1:p.Ile181Arg
|
|
ENST00000476923.1:n.269T>G
|
|
|
ENST00000484913.5:n.1547T>G
|
|
|
NM_000466.2:c.1508T>G
|
NP_000457.1:p.Ile503Arg
|
|
NM_001282677.1:c.1508T>G
|
NP_001269606.1:p.Ile503Arg
|
|
NM_001282678.1:c.884T>G
|
NP_001269607.1:p.Ile295Arg
|
|
XM_005250433.3:c.-159T>G
|
XP_005250490.1:n.-159T>G
|
|
XR_242246.3:n.1604T>G
|
|
|
XM_017012319.2:c.-159T>G
|
XP_016867808.1:n.-159T>G
|
|
XR_001744808.2:n.618T>G
|
|
|
XR_242246.5:n.1555T>G
|
|
|
NM_000466.3:c.1508T>G
MANE Select
|
NP_000457.1:p.Ile503Arg
|
|
NM_001282677.2:c.1508T>G
|
NP_001269606.1:p.Ile503Arg
|
|
NM_001282678.2:c.884T>G
|
NP_001269607.1:p.Ile295Arg
|
|