ENST00000691183.1:c.354T>C
|
ENSP00000509954.1:p.Gly118=
|
|
ENST00000378842.8:c.403T>C
MANE Select
|
ENSP00000368119.4:p.Ser135Pro
|
|
ENST00000378842.7:c.403T>C
|
ENSP00000368119.3:p.Ser135Pro
|
|
ENST00000450095.6:c.76T>C
|
ENSP00000401956.2:p.Ser26Pro
|
|
ENST00000465543.6:n.742T>C
|
|
|
ENST00000472111.5:n.659T>C
|
|
|
ENST00000473506.6:c.354T>C
|
ENSP00000432839.2:p.Gly118=
|
|
ENST00000473529.5:n.539T>C
|
|
|
ENST00000485531.1:n.844T>C
|
|
|
ENST00000487381.5:n.788T>C
|
|
|
ENST00000489643.6:n.283-258T>C
|
|
|
ENST00000554085.5:c.*147T>C
|
ENSP00000450419.1:n.*147T>C
|
|
ENST00000554139.5:n.582T>C
|
|
|
ENST00000554550.5:c.*23T>C
|
ENSP00000451435.1:n.*23T>C
|
|
ENST00000554638.5:n.875T>C
|
|
|
ENST00000554897.5:c.*23T>C
|
ENSP00000450942.1:n.*23T>C
|
|
ENST00000554944.5:n.599T>C
|
|
|
ENST00000555020.5:n.559T>C
|
|
|
ENST00000555086.5:n.407T>C
|
|
|
ENST00000555214.5:n.262-191T>C
|
|
|
ENST00000556244.1:c.390T>C
|
|
|
ENST00000556278.1:c.253-258T>C
|
ENSP00000451792.1:n.253-258T>C
|
|
ENST00000556494.5:n.524T>C
|
|
|
ENST00000557541.5:n.547T>C
|
|
|
ENST00000557706.5:n.965T>C
|
|
|
NM_000155.3:c.403T>C
|
NP_000146.2:p.Ser135Pro
|
|
NM_001258332.1:c.76T>C
|
NP_001245261.1:p.Ser26Pro
|
|
NM_000155.4:c.403T>C
MANE Select
|
NP_000146.2:p.Ser135Pro
|
|
NM_001258332.2:c.76T>C
|
NP_001245261.1:p.Ser26Pro
|
|