ENST00000264595.7:c.317G>T
MANE Select
|
ENSP00000264595.2:p.Arg106Ile
|
|
ENST00000264595.6:c.317G>T
|
ENSP00000264595.2:p.Arg106Ile
|
|
ENST00000506853.5:n.351G>T
|
|
|
ENST00000510635.1:c.13G>T
|
|
|
ENST00000510955.5:n.315+620G>T
|
|
|
NM_000027.3:c.317G>T
|
NP_000018.2:p.Arg106Ile
|
|
NM_001171988.1:c.317G>T
|
NP_001165459.1:p.Arg106Ile
|
|
NR_033655.1:n.445G>T
|
|
|
XM_006714123.2:c.317G>T
|
XP_006714186.1:p.Arg106Ile
|
|
XR_001741155.2:n.411G>T
|
|
|
NM_000027.4:c.317G>T
MANE Select
|
NP_000018.2:p.Arg106Ile
|
|
NM_001171988.2:c.317G>T
|
NP_001165459.1:p.Arg106Ile
|
|
NR_033655.2:n.379G>T
|
|
|