|
NM_033100.4:c.1511G>A
MANE Select
|
NP_149091.1:p.Trp504Ter
|
|
ENST00000623527.4:c.1511G>A
MANE Select
|
ENSP00000485478.1:p.Trp504Ter
|
|
NM_001171971.2:c.1511G>A
|
NP_001165442.1:p.Trp504Ter
|
|
NM_001171971.3:c.1511G>A
|
NP_001165442.1:p.Trp504Ter
|
|
NM_033100.3:c.1511G>A
|
NP_149091.1:p.Trp504Ter
|
|
ENST00000332904.7:c.1511G>A
|
ENSP00000331063.3:p.Trp504Ter
|
|
ENST00000372117.6:c.726G>A
|
|
|
ENST00000622973.1:c.244G>A
|
|
|
ENST00000623527.3:c.1511G>A
|
ENSP00000485478.1:p.Trp504Ter
|
|
XM_011540337.1:c.1685G>A
|
XP_011538639.1:p.Trp562Ter
|
|
XM_011540338.1:c.1685G>A
|
XP_011538640.1:p.Trp562Ter
|
|
XM_011540339.1:c.1064G>A
|
XP_011538641.1:p.Trp355Ter
|
|
XM_011540340.1:c.1685G>A
|
XP_011538642.1:p.Trp562Ter
|
|
XM_011540340.3:c.1685G>A
|
XP_011538642.1:p.Trp562Ter
|