|
NM_033100.4:c.983C>T
MANE Select
|
NP_149091.1:p.Ala328Val
|
|
ENST00000623527.4:c.983C>T
MANE Select
|
ENSP00000485478.1:p.Ala328Val
|
|
NM_001171971.2:c.983C>T
|
NP_001165442.1:p.Ala328Val
|
|
NM_001171971.3:c.983C>T
|
NP_001165442.1:p.Ala328Val
|
|
NM_033100.3:c.983C>T
|
NP_149091.1:p.Ala328Val
|
|
ENST00000332904.7:c.983C>T
|
ENSP00000331063.3:p.Ala328Val
|
|
ENST00000372117.6:c.363C>T
|
|
|
ENST00000623527.3:c.983C>T
|
ENSP00000485478.1:p.Ala328Val
|
|
ENST00000624091.1:c.269C>T
|
|
|
XM_011540337.1:c.1157C>T
|
XP_011538639.1:p.Ala386Val
|
|
XM_011540338.1:c.1157C>T
|
XP_011538640.1:p.Ala386Val
|
|
XM_011540339.1:c.536C>T
|
XP_011538641.1:p.Ala179Val
|
|
XM_011540340.1:c.1157C>T
|
XP_011538642.1:p.Ala386Val
|
|
XM_011540340.3:c.1157C>T
|
XP_011538642.1:p.Ala386Val
|