ENST00000682114.1:c.406G>C
|
ENSP00000507245.1:p.Asp136His
|
|
ENST00000682478.1:n.596G>C
|
|
|
ENST00000683576.1:n.596G>C
|
|
|
ENST00000683627.1:c.406G>C
|
ENSP00000507533.1:p.Asp136His
|
|
ENST00000684082.1:c.363G>C
|
ENSP00000508266.1:n.363G>C
|
|
ENST00000684633.1:n.378G>C
|
|
|
ENST00000684678.1:c.402G>C
|
ENSP00000507059.1:n.402G>C
|
|
ENST00000369842.9:c.406G>C
MANE Select
|
ENSP00000358857.4:p.Asp136His
|
|
ENST00000369835.3:c.301G>C
|
ENSP00000358850.3:p.Asp101His
|
|
ENST00000369842.8:c.406G>C
|
ENSP00000358857.4:p.Asp136His
|
|
ENST00000428228.5:c.*311G>C
|
ENSP00000401081.1:n.*311G>C
|
|
ENST00000468294.5:n.366G>C
|
|
|
ENST00000471965.1:n.195G>C
|
|
|
ENST00000485261.1:n.596G>C
|
|
|
ENST00000486738.5:n.764G>C
|
|
|
ENST00000492448.1:n.389G>C
|
|
|
NM_000117.2:c.406G>C , LRG_745t1:c.406G>C
|
NP_000108.1:p.Asp136His
|
|
XM_024452349.1:c.412G>C
|
XP_024308117.1:p.Asp138His
|
|
NM_000117.3:c.406G>C
MANE Select
|
NP_000108.1:p.Asp136His
|
|