ENST00000649865.1:c.*3129G>C
|
ENSP00000496919.1:n.*3129G>C
|
|
ENST00000650285.1:c.*3129G>C
MANE Select
|
ENSP00000497069.1:n.*3129G>C
|
|
ENST00000268035.10:c.*3129G>C
|
ENSP00000268035.6:n.*3129G>C
|
|
ENST00000558762.5:c.*3129G>C
|
ENSP00000453007.1:n.*3129G>C
|
|
NM_000875.4:c.*3129G>C
|
NP_000866.1:n.*3129G>C
|
|
NM_001291858.1:c.*3129G>C
|
NP_001278787.1:n.*3129G>C
|
|
XM_011521513.1:c.*3129G>C
|
XP_011519815.1:n.*3129G>C
|
|
XM_011521514.1:c.*2643G>C
|
XP_011519816.1:n.*2643G>C
|
|
XM_011521515.1:c.*3129G>C
|
XP_011519817.1:n.*3129G>C
|
|
XM_011521516.1:c.*3129G>C
|
XP_011519818.1:n.*3129G>C
|
|
XM_011521517.1:c.*3129G>C
|
XP_011519819.1:n.*3129G>C
|
|
XM_017022136.1:c.*3129G>C
|
XP_016877625.1:n.*3129G>C
|
|
XM_017022137.1:c.*2643G>C
|
XP_016877626.1:n.*2643G>C
|
|
XM_017022138.1:c.*3129G>C
|
XP_016877627.1:n.*3129G>C
|
|
NM_000875.5:c.*3129G>C
MANE Select
|
NP_000866.1:n.*3129G>C
|
|
NM_001291858.2:c.*3129G>C
|
NP_001278787.1:n.*3129G>C
|
|