ENST00000262461.7:c.3578A>T
MANE Select
|
ENSP00000262461.2:p.Asp1193Val
|
|
ENST00000262461.6:c.3578A>T
|
ENSP00000262461.2:p.Asp1193Val
|
|
ENST00000343225.4:c.3530A>T
|
ENSP00000340878.4:p.Asp1177Val
|
|
ENST00000509205.5:c.*191A>T
|
ENSP00000427109.1:n.*191A>T
|
|
NM_001046.2:c.3578A>T
|
NP_001037.1:p.Asp1193Val
|
|
NM_001256461.1:c.3530A>T
|
NP_001243390.1:p.Asp1177Val
|
|
NR_046207.1:n.3808A>T
|
|
|
XM_017009771.1:c.1820A>T
|
XP_016865260.1:p.Asp607Val
|
|
XR_001742214.1:n.3802A>T
|
|
|
NM_001046.3:c.3578A>T
MANE Select
|
NP_001037.1:p.Asp1193Val
|
|
NM_001256461.2:c.3530A>T
|
NP_001243390.1:p.Asp1177Val
|
|
NR_046207.2:n.3833A>T
|
|
|