ENST00000269980.7:c.1326C>G
MANE Select
|
ENSP00000269980.2:p.His442Gln
|
|
ENST00000269980.6:c.1326C>G
|
ENSP00000269980.2:p.His442Gln
|
|
ENST00000457836.6:c.1335C>G
|
ENSP00000416000.2:p.His445Gln
|
|
ENST00000540732.3:c.1428C>G
|
ENSP00000443246.1:p.His476Gln
|
|
ENST00000544905.1:c.156C>G
|
|
|
ENST00000595085.5:c.922+1899C>G
|
ENSP00000471150.2:n.922+1899C>G
|
|
NM_000709.3:c.1326C>G
|
NP_000700.1:p.His442Gln
|
|
NM_001164783.1:c.1323C>G
|
NP_001158255.1:p.His441Gln
|
|
NM_000709.4:c.1326C>G
MANE Select
|
NP_000700.1:p.His442Gln
|
|
NM_001164783.2:c.1323C>G
|
NP_001158255.1:p.His441Gln
|
|