ENST00000269980.7:c.123G>C
MANE Select
|
ENSP00000269980.2:p.Gln41His
|
|
ENST00000269980.6:c.123G>C
|
ENSP00000269980.2:p.Gln41His
|
|
ENST00000457836.6:c.58-1G>C
|
ENSP00000416000.2:n.58-1G>C
|
|
ENST00000538423.5:n.143G>C
|
|
|
ENST00000540732.3:c.225G>C
|
ENSP00000443246.1:p.Gln75His
|
|
ENST00000542943.5:c.123G>C
|
ENSP00000440345.1:p.Gln41His
|
|
ENST00000595085.5:c.123G>C
|
ENSP00000471150.2:p.Gln41His
|
|
ENST00000604424.1:n.365G>C
|
|
|
NM_000709.3:c.123G>C
|
NP_000700.1:p.Gln41His
|
|
NM_001164783.1:c.123G>C
|
NP_001158255.1:p.Gln41His
|
|
NM_000709.4:c.123G>C
MANE Select
|
NP_000700.1:p.Gln41His
|
|
NM_001164783.2:c.123G>C
|
NP_001158255.1:p.Gln41His
|
|