ENST00000691183.1:c.*165A>G
|
ENSP00000509954.1:n.*165A>G
|
|
ENST00000378842.8:c.577A>G
MANE Select
|
ENSP00000368119.4:p.Ser193Gly
|
|
ENST00000378842.7:c.577A>G
|
ENSP00000368119.3:p.Ser193Gly
|
|
ENST00000450095.6:c.250A>G
|
ENSP00000401956.2:p.Ser84Gly
|
|
ENST00000472111.5:n.833A>G
|
|
|
ENST00000473506.6:c.*165A>G
|
ENSP00000432839.2:n.*165A>G
|
|
ENST00000473529.5:n.736A>G
|
|
|
ENST00000485531.1:n.1171A>G
|
|
|
ENST00000487381.5:n.962A>G
|
|
|
ENST00000489643.6:n.352A>G
|
|
|
ENST00000554085.5:c.*321A>G
|
ENSP00000450419.1:n.*321A>G
|
|
ENST00000554139.5:n.823A>G
|
|
|
ENST00000554550.5:c.*197A>G
|
ENSP00000451435.1:n.*197A>G
|
|
ENST00000554638.5:n.1049A>G
|
|
|
ENST00000554897.5:c.*264A>G
|
ENSP00000450942.1:n.*264A>G
|
|
ENST00000554944.5:n.926A>G
|
|
|
ENST00000555020.5:n.733A>G
|
|
|
ENST00000555086.5:n.581A>G
|
|
|
ENST00000555214.5:n.398A>G
|
|
|
ENST00000556244.1:c.564A>G
|
|
|
ENST00000556278.1:c.322A>G
|
ENSP00000451792.1:p.Ser108Gly
|
|
ENST00000556494.5:n.698A>G
|
|
|
ENST00000557706.5:n.1139A>G
|
|
|
NM_000155.3:c.577A>G
|
NP_000146.2:p.Ser193Gly
|
|
NM_001258332.1:c.250A>G
|
NP_001245261.1:p.Ser84Gly
|
|
NM_000155.4:c.577A>G
MANE Select
|
NP_000146.2:p.Ser193Gly
|
|
NM_001258332.2:c.250A>G
|
NP_001245261.1:p.Ser84Gly
|
|