ENST00000463045.3:c.336G>T
|
ENSP00000481376.2:p.Gln112His
|
|
ENST00000491274.6:c.465G>T
|
ENSP00000480482.2:p.Gln155His
|
|
ENST00000375499.8:c.507G>T
MANE Select
|
ENSP00000364649.3:p.Gln169His
|
|
ENST00000375499.7:c.507G>T
|
ENSP00000364649.3:p.Gln169His
|
|
ENST00000463045.2:c.336G>T
|
ENSP00000481376.1:p.Gln112His
|
|
ENST00000475506.1:n.424G>T
|
|
|
ENST00000485515.5:n.441G>T
|
|
|
ENST00000491274.5:c.465G>T
|
ENSP00000480482.1:p.Gln155His
|
|
NM_003000.2:c.507G>T , LRG_316t1:c.507G>T
|
NP_002991.2:p.Gln169His
|
|
NM_003000.3:c.507G>T
MANE Select
|
NP_002991.2:p.Gln169His
|
|