ENST00000691183.1:c.*302C>G
|
ENSP00000509954.1:n.*302C>G
|
|
ENST00000378842.8:c.714C>G
MANE Select
|
ENSP00000368119.4:p.His238Gln
|
|
ENST00000378842.7:c.714C>G
|
ENSP00000368119.3:p.His238Gln
|
|
ENST00000450095.6:c.387C>G
|
ENSP00000401956.2:p.His129Gln
|
|
ENST00000473506.6:c.*302C>G
|
ENSP00000432839.2:n.*302C>G
|
|
ENST00000473529.5:n.873C>G
|
|
|
ENST00000487381.5:n.1404C>G
|
|
|
ENST00000489643.6:n.794C>G
|
|
|
ENST00000554085.5:c.*458C>G
|
ENSP00000450419.1:n.*458C>G
|
|
ENST00000554550.5:c.*334C>G
|
ENSP00000451435.1:n.*334C>G
|
|
ENST00000554638.5:n.1186C>G
|
|
|
ENST00000555020.5:n.1175C>G
|
|
|
ENST00000555086.5:n.718C>G
|
|
|
ENST00000555754.1:n.59C>G
|
|
|
ENST00000556244.1:c.701C>G
|
|
|
ENST00000556278.1:c.432+332C>G
|
ENSP00000451792.1:n.432+332C>G
|
|
ENST00000557706.5:n.1276C>G
|
|
|
NM_000155.3:c.714C>G
|
NP_000146.2:p.His238Gln
|
|
NM_001258332.1:c.387C>G
|
NP_001245261.1:p.His129Gln
|
|
NM_000155.4:c.714C>G
MANE Select
|
NP_000146.2:p.His238Gln
|
|
NM_001258332.2:c.387C>G
|
NP_001245261.1:p.His129Gln
|
|