ENST00000324856.13:c.5173A>T
MANE Select
|
ENSP00000320485.7:p.Ile1725Phe
|
|
ENST00000374152.7:c.4024A>T
|
ENSP00000363267.2:p.Ile1342Phe
|
|
ENST00000430799.7:c.4021A>T
|
ENSP00000390317.3:p.Ile1341Phe
|
|
ENST00000466382.2:c.590A>T
|
|
|
ENST00000636219.1:c.4027A>T
|
ENSP00000489842.1:p.Ile1343Phe
|
|
ENST00000637788.1:n.973A>T
|
|
|
ENST00000324856.11:c.5173A>T
|
ENSP00000320485.7:p.Ile1725Phe
|
|
ENST00000374152.6:c.4024A>T
|
ENSP00000363267.2:p.Ile1342Phe
|
|
ENST00000430799.6:c.1862A>T
|
|
|
ENST00000457599.6:c.4522A>T
|
ENSP00000387636.2:p.Ile1508Phe
|
|
ENST00000466382.1:c.590A>T
|
|
|
ENST00000532781.1:c.671A>T
|
|
|
NM_006015.4:c.5173A>T , LRG_875t1:c.5173A>T
|
NP_006006.3:p.Ile1725Phe
|
|
NM_139135.2:c.4522A>T
|
NP_624361.1:p.Ile1508Phe
|
|
NM_006015.5:c.5173A>T
|
NP_006006.3:p.Ile1725Phe
|
|
NM_139135.3:c.4522A>T
|
NP_624361.1:p.Ile1508Phe
|
|
NM_006015.6:c.5173A>T
MANE Select
|
NP_006006.3:p.Ile1725Phe
|
|
NM_139135.4:c.4522A>T
|
NP_624361.1:p.Ile1508Phe
|
|