ENST00000463045.3:c.286A>T
|
ENSP00000481376.2:p.Ile96Phe
|
|
ENST00000491274.6:c.415A>T
|
ENSP00000480482.2:p.Ile139Phe
|
|
ENST00000375499.8:c.457A>T
MANE Select
|
ENSP00000364649.3:p.Ile153Phe
|
|
ENST00000375499.7:c.457A>T
|
ENSP00000364649.3:p.Ile153Phe
|
|
ENST00000463045.2:c.286A>T
|
ENSP00000481376.1:p.Ile96Phe
|
|
ENST00000475506.1:n.374A>T
|
|
|
ENST00000485515.5:n.391A>T
|
|
|
ENST00000491274.5:c.415A>T
|
ENSP00000480482.1:p.Ile139Phe
|
|
NM_003000.2:c.457A>T , LRG_316t1:c.457A>T
|
NP_002991.2:p.Ile153Phe
|
|
NM_003000.3:c.457A>T
MANE Select
|
NP_002991.2:p.Ile153Phe
|
|