ENST00000368985.8:c.991A>T
MANE Select
|
ENSP00000357981.3:p.Ile331Phe
|
|
ENST00000448301.7:c.763A>T
|
ENSP00000408414.2:p.Ile255Phe
|
|
ENST00000472977.7:c.991A>T
|
ENSP00000475176.2:p.Ile331Phe
|
|
ENST00000483930.2:c.*185A>T
|
ENSP00000475812.2:n.*185A>T
|
|
ENST00000607427.2:c.991A>T
|
ENSP00000475557.2:p.Ile331Phe
|
|
ENST00000679512.1:c.888A>T
|
ENSP00000505113.1:p.Lys296Asn
|
|
ENST00000679898.1:c.718A>T
|
ENSP00000505326.1:p.Ile240Phe
|
|
ENST00000680288.1:c.841A>T
|
ENSP00000506001.1:p.Ile281Phe
|
|
ENST00000680311.1:c.*74A>T
|
ENSP00000505020.1:n.*74A>T
|
|
ENST00000680471.1:c.*162A>T
|
ENSP00000506603.1:n.*162A>T
|
|
ENST00000680664.1:c.814A>T
|
ENSP00000506248.1:p.Ile272Phe
|
|
ENST00000680931.1:c.*341A>T
|
ENSP00000504934.1:n.*341A>T
|
|
ENST00000681357.1:n.381A>T
|
|
|
ENST00000681444.1:c.991A>T
|
ENSP00000505359.1:p.Ile331Phe
|
|
ENST00000368985.7:c.991A>T
|
ENSP00000357981.3:p.Ile331Phe
|
|
ENST00000448301.6:c.841A>T
|
ENSP00000408414.1:p.Ile281Phe
|
|
ENST00000472977.6:c.284A>T
|
|
|
ENST00000483930.1:c.539A>T
|
ENSP00000475812.1:n.539A>T
|
|
ENST00000607427.1:c.12A>T
|
|
|
NM_001199739.1:c.841A>T
|
NP_001186668.1:p.Ile281Phe
|
|
NM_004079.4:c.991A>T
|
NP_004070.3:p.Ile331Phe
|
|
NM_004079.5:c.991A>T
MANE Select
|
NP_004070.3:p.Ile331Phe
|
|
NM_001199739.2:c.841A>T
|
NP_001186668.1:p.Ile281Phe
|
|