ENST00000691183.1:c.348C>G
|
ENSP00000509954.1:p.Thr116=
|
|
ENST00000378842.8:c.397C>G
MANE Select
|
ENSP00000368119.4:p.Pro133Ala
|
|
ENST00000378842.7:c.397C>G
|
ENSP00000368119.3:p.Pro133Ala
|
|
ENST00000450095.6:c.70C>G
|
ENSP00000401956.2:p.Pro24Ala
|
|
ENST00000465543.6:n.736C>G
|
|
|
ENST00000472111.5:n.653C>G
|
|
|
ENST00000473506.6:c.348C>G
|
ENSP00000432839.2:p.Thr116=
|
|
ENST00000473529.5:n.533C>G
|
|
|
ENST00000485531.1:n.838C>G
|
|
|
ENST00000487381.5:n.782C>G
|
|
|
ENST00000489643.6:n.283-264C>G
|
|
|
ENST00000554085.5:c.*141C>G
|
ENSP00000450419.1:n.*141C>G
|
|
ENST00000554139.5:n.576C>G
|
|
|
ENST00000554550.5:c.*17C>G
|
ENSP00000451435.1:n.*17C>G
|
|
ENST00000554638.5:n.869C>G
|
|
|
ENST00000554897.5:c.*17C>G
|
ENSP00000450942.1:n.*17C>G
|
|
ENST00000554944.5:n.593C>G
|
|
|
ENST00000555020.5:n.553C>G
|
|
|
ENST00000555086.5:n.401C>G
|
|
|
ENST00000555214.5:n.262-197C>G
|
|
|
ENST00000556244.1:c.384C>G
|
|
|
ENST00000556278.1:c.253-264C>G
|
ENSP00000451792.1:n.253-264C>G
|
|
ENST00000556494.5:n.518C>G
|
|
|
ENST00000557541.5:n.541C>G
|
|
|
ENST00000557706.5:n.959C>G
|
|
|
NM_000155.3:c.397C>G
|
NP_000146.2:p.Pro133Ala
|
|
NM_001258332.1:c.70C>G
|
NP_001245261.1:p.Pro24Ala
|
|
NM_000155.4:c.397C>G
MANE Select
|
NP_000146.2:p.Pro133Ala
|
|
NM_001258332.2:c.70C>G
|
NP_001245261.1:p.Pro24Ala
|
|