ENST00000691183.1:c.*330A>G
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ENSP00000509954.1:n.*330A>G
|
|
ENST00000378842.8:c.742A>G
MANE Select
|
ENSP00000368119.4:p.Thr248Ala
|
|
ENST00000378842.7:c.742A>G
|
ENSP00000368119.3:p.Thr248Ala
|
|
ENST00000450095.6:c.415A>G
|
ENSP00000401956.2:p.Thr139Ala
|
|
ENST00000473506.6:c.*330A>G
|
ENSP00000432839.2:n.*330A>G
|
|
ENST00000473529.5:n.901A>G
|
|
|
ENST00000487381.5:n.1432A>G
|
|
|
ENST00000489643.6:n.822A>G
|
|
|
ENST00000554085.5:c.*486A>G
|
ENSP00000450419.1:n.*486A>G
|
|
ENST00000554550.5:c.*362A>G
|
ENSP00000451435.1:n.*362A>G
|
|
ENST00000554638.5:n.1214A>G
|
|
|
ENST00000555020.5:n.1203A>G
|
|
|
ENST00000555086.5:n.746A>G
|
|
|
ENST00000555754.1:n.87A>G
|
|
|
ENST00000556244.1:c.729A>G
|
|
|
ENST00000556278.1:c.432+360A>G
|
ENSP00000451792.1:n.432+360A>G
|
|
ENST00000557706.5:n.1304A>G
|
|
|
NM_000155.3:c.742A>G
|
NP_000146.2:p.Thr248Ala
|
|
NM_001258332.1:c.415A>G
|
NP_001245261.1:p.Thr139Ala
|
|
NM_000155.4:c.742A>G
MANE Select
|
NP_000146.2:p.Thr248Ala
|
|
NM_001258332.2:c.415A>G
|
NP_001245261.1:p.Thr139Ala
|
|