ENST00000463045.3:c.276G>C
|
ENSP00000481376.2:p.Gln92His
|
|
ENST00000491274.6:c.405G>C
|
ENSP00000480482.2:p.Gln135His
|
|
ENST00000375499.8:c.447G>C
MANE Select
|
ENSP00000364649.3:p.Gln149His
|
|
ENST00000375499.7:c.447G>C
|
ENSP00000364649.3:p.Gln149His
|
|
ENST00000463045.2:c.276G>C
|
ENSP00000481376.1:p.Gln92His
|
|
ENST00000475506.1:n.364G>C
|
|
|
ENST00000485515.5:n.381G>C
|
|
|
ENST00000491274.5:c.405G>C
|
ENSP00000480482.1:p.Gln135His
|
|
NM_003000.2:c.447G>C , LRG_316t1:c.447G>C
|
NP_002991.2:p.Gln149His
|
|
NM_003000.3:c.447G>C
MANE Select
|
NP_002991.2:p.Gln149His
|
|