ENST00000436784.7:c.*1T>G
MANE Select
|
ENSP00000389175.2:n.*1T>G
|
|
ENST00000436784.6:c.*1T>G
|
ENSP00000389175.2:n.*1T>G
|
|
ENST00000461183.5:c.845T>G
|
ENSP00000417264.1:p.Met282Arg
|
|
ENST00000471180.5:c.716T>G
|
ENSP00000417526.1:p.Met239Arg
|
|
ENST00000473032.5:c.611T>G
|
ENSP00000418951.1:p.Met204Arg
|
|
ENST00000486393.5:c.*936T>G
|
ENSP00000419868.1:n.*936T>G
|
|
ENST00000489173.1:n.1867T>G
|
|
|
NM_145262.3:c.*1T>G
|
NP_660305.2:n.*1T>G
|
|
NR_026699.1:n.1671T>G
|
|
|
NR_026700.1:n.777T>G
|
|
|
NR_026701.1:n.1669T>G
|
|
|
NR_026702.1:n.707T>G
|
|
|
XM_005264878.2:c.*692T>G
|
XP_005264935.1:n.*692T>G
|
|
XR_245095.2:n.2824T>G
|
|
|
XM_017005730.1:c.*1T>G
|
XP_016861219.1:n.*1T>G
|
|
XM_024453351.1:c.*1T>G
|
XP_024309119.1:n.*1T>G
|
|
XM_024453352.1:c.*692T>G
|
XP_024309120.1:n.*692T>G
|
|
XR_001740022.2:n.3475T>G
|
|
|
XR_001740023.2:n.2999T>G
|
|
|
XR_245095.4:n.2825T>G
|
|
|
NM_145262.4:c.*1T>G
MANE Select
|
NP_660305.2:n.*1T>G
|
|
NR_026699.2:n.1663T>G
|
|
|
NR_026700.2:n.769T>G
|
|
|
NR_026701.2:n.1661T>G
|
|
|
NR_026702.2:n.699T>G
|
|
|
NM_001144951.2:c.*692T>G
|
NP_001138423.1:n.*692T>G
|
|