ENST00000436784.7:c.*192G>A
MANE Select
|
ENSP00000389175.2:n.*192G>A
|
|
ENST00000436784.6:c.*192G>A
|
ENSP00000389175.2:n.*192G>A
|
|
ENST00000471180.5:c.*70G>A
|
ENSP00000417526.1:n.*70G>A
|
|
ENST00000473032.5:c.*70G>A
|
ENSP00000418951.1:n.*70G>A
|
|
ENST00000486393.5:c.*1127G>A
|
ENSP00000419868.1:n.*1127G>A
|
|
ENST00000489173.1:n.1926G>A
|
|
|
NM_145262.3:c.*192G>A
|
NP_660305.2:n.*192G>A
|
|
NR_026699.1:n.1862G>A
|
|
|
NR_026700.1:n.854G>A
|
|
|
NR_026701.1:n.1746G>A
|
|
|
NR_026702.1:n.784G>A
|
|
|
XM_005264878.2:c.*883G>A
|
XP_005264935.1:n.*883G>A
|
|
XR_245095.2:n.2901G>A
|
|
|
XM_017005730.1:c.*192G>A
|
XP_016861219.1:n.*192G>A
|
|
XM_024453351.1:c.*192G>A
|
XP_024309119.1:n.*192G>A
|
|
XM_024453352.1:c.*883G>A
|
XP_024309120.1:n.*883G>A
|
|
XR_001740022.2:n.3552G>A
|
|
|
XR_001740023.2:n.3076G>A
|
|
|
XR_245095.4:n.2902G>A
|
|
|
NM_145262.4:c.*192G>A
MANE Select
|
NP_660305.2:n.*192G>A
|
|
NR_026699.2:n.1854G>A
|
|
|
NR_026700.2:n.846G>A
|
|
|
NR_026701.2:n.1738G>A
|
|
|
NR_026702.2:n.776G>A
|
|
|
NM_001144951.2:c.*883G>A
|
NP_001138423.1:n.*883G>A
|
|