ENST00000264595.7:c.593C>T
MANE Select
|
ENSP00000264595.2:p.Thr198Ile
|
|
ENST00000264595.6:c.593C>T
|
ENSP00000264595.2:p.Thr198Ile
|
|
ENST00000502310.5:c.248C>T
|
ENSP00000423798.1:p.Thr83Ile
|
|
ENST00000506853.5:n.627C>T
|
|
|
ENST00000510635.1:c.289C>T
|
|
|
ENST00000510955.5:n.514C>T
|
|
|
NM_000027.3:c.593C>T
|
NP_000018.2:p.Thr198Ile
|
|
NM_001171988.1:c.593C>T
|
NP_001165459.1:p.Thr198Ile
|
|
NR_033655.1:n.721C>T
|
|
|
XM_006714123.2:c.593C>T
|
XP_006714186.1:p.Thr198Ile
|
|
XR_001741155.2:n.687C>T
|
|
|
NM_000027.4:c.593C>T
MANE Select
|
NP_000018.2:p.Thr198Ile
|
|
NM_001171988.2:c.593C>T
|
NP_001165459.1:p.Thr198Ile
|
|
NR_033655.2:n.655C>T
|
|
|