ENST00000436784.7:c.*193A>G
MANE Select
|
ENSP00000389175.2:n.*193A>G
|
|
ENST00000436784.6:c.*193A>G
|
ENSP00000389175.2:n.*193A>G
|
|
ENST00000471180.5:c.*71A>G
|
ENSP00000417526.1:n.*71A>G
|
|
ENST00000473032.5:c.*71A>G
|
ENSP00000418951.1:n.*71A>G
|
|
ENST00000486393.5:c.*1128A>G
|
ENSP00000419868.1:n.*1128A>G
|
|
ENST00000489173.1:n.1927A>G
|
|
|
NM_145262.3:c.*193A>G
|
NP_660305.2:n.*193A>G
|
|
NR_026699.1:n.1863A>G
|
|
|
NR_026700.1:n.855A>G
|
|
|
NR_026701.1:n.1747A>G
|
|
|
NR_026702.1:n.785A>G
|
|
|
XM_005264878.2:c.*884A>G
|
XP_005264935.1:n.*884A>G
|
|
XR_245095.2:n.2902A>G
|
|
|
XM_017005730.1:c.*193A>G
|
XP_016861219.1:n.*193A>G
|
|
XM_024453351.1:c.*193A>G
|
XP_024309119.1:n.*193A>G
|
|
XM_024453352.1:c.*884A>G
|
XP_024309120.1:n.*884A>G
|
|
XR_001740022.2:n.3553A>G
|
|
|
XR_001740023.2:n.3077A>G
|
|
|
XR_245095.4:n.2903A>G
|
|
|
NM_145262.4:c.*193A>G
MANE Select
|
NP_660305.2:n.*193A>G
|
|
NR_026699.2:n.1855A>G
|
|
|
NR_026700.2:n.847A>G
|
|
|
NR_026701.2:n.1739A>G
|
|
|
NR_026702.2:n.777A>G
|
|
|
NM_001144951.2:c.*884A>G
|
NP_001138423.1:n.*884A>G
|
|