ENST00000691183.1:c.*163G>C
|
ENSP00000509954.1:n.*163G>C
|
|
ENST00000378842.8:c.575G>C
MANE Select
|
ENSP00000368119.4:p.Ser192Thr
|
|
ENST00000378842.7:c.575G>C
|
ENSP00000368119.3:p.Ser192Thr
|
|
ENST00000450095.6:c.248G>C
|
ENSP00000401956.2:p.Ser83Thr
|
|
ENST00000472111.5:n.831G>C
|
|
|
ENST00000473506.6:c.*163G>C
|
ENSP00000432839.2:n.*163G>C
|
|
ENST00000473529.5:n.734G>C
|
|
|
ENST00000485531.1:n.1169G>C
|
|
|
ENST00000487381.5:n.960G>C
|
|
|
ENST00000489643.6:n.350G>C
|
|
|
ENST00000554085.5:c.*319G>C
|
ENSP00000450419.1:n.*319G>C
|
|
ENST00000554139.5:n.821G>C
|
|
|
ENST00000554550.5:c.*195G>C
|
ENSP00000451435.1:n.*195G>C
|
|
ENST00000554638.5:n.1047G>C
|
|
|
ENST00000554897.5:c.*262G>C
|
ENSP00000450942.1:n.*262G>C
|
|
ENST00000554944.5:n.924G>C
|
|
|
ENST00000555020.5:n.731G>C
|
|
|
ENST00000555086.5:n.579G>C
|
|
|
ENST00000555214.5:n.396G>C
|
|
|
ENST00000556244.1:c.562G>C
|
|
|
ENST00000556278.1:c.320G>C
|
ENSP00000451792.1:p.Ser107Thr
|
|
ENST00000556494.5:n.696G>C
|
|
|
ENST00000557706.5:n.1137G>C
|
|
|
NM_000155.3:c.575G>C
|
NP_000146.2:p.Ser192Thr
|
|
NM_001258332.1:c.248G>C
|
NP_001245261.1:p.Ser83Thr
|
|
NM_000155.4:c.575G>C
MANE Select
|
NP_000146.2:p.Ser192Thr
|
|
NM_001258332.2:c.248G>C
|
NP_001245261.1:p.Ser83Thr
|
|