|
NM_033100.4:c.2229G>A
MANE Select
|
NP_149091.1:p.Arg743=
|
|
ENST00000623527.4:c.2229G>A
MANE Select
|
ENSP00000485478.1:p.Arg743=
|
|
NM_001171971.2:c.2040+922G>A
|
NP_001165442.1:n.2040+922G>A
|
|
NM_001171971.3:c.2040+922G>A
|
NP_001165442.1:n.2040+922G>A
|
|
NM_033100.3:c.2229G>A
|
NP_149091.1:p.Arg743=
|
|
ENST00000332904.7:c.2040+922G>A
|
ENSP00000331063.3:n.2040+922G>A
|
|
ENST00000372117.6:c.1444G>A
|
|
|
ENST00000459673.1:n.661G>A
|
|
|
ENST00000623399.1:c.211+922G>A
|
|
|
ENST00000623527.3:c.2229G>A
|
ENSP00000485478.1:p.Arg743=
|
|
XM_011540337.1:c.2403G>A
|
XP_011538639.1:p.Arg801=
|
|
XM_011540338.1:c.2214+922G>A
|
XP_011538640.1:n.2214+922G>A
|
|
XM_011540339.1:c.1782G>A
|
XP_011538641.1:p.Arg594=
|