ENST00000436784.7:c.1300T>G
MANE Select
|
ENSP00000389175.2:p.Leu434Val
|
|
ENST00000305690.12:c.*419T>G
|
ENSP00000301965.9:n.*419T>G
|
|
ENST00000436784.6:c.1300T>G
|
ENSP00000389175.2:p.Leu434Val
|
|
ENST00000461183.5:c.764-192T>G
|
ENSP00000417264.1:n.764-192T>G
|
|
ENST00000471180.5:c.635-192T>G
|
ENSP00000417526.1:n.635-192T>G
|
|
ENST00000473032.5:c.530-192T>G
|
ENSP00000418951.1:n.530-192T>G
|
|
ENST00000477382.1:c.*419T>G
|
ENSP00000419008.1:n.*419T>G
|
|
ENST00000486393.5:c.*663T>G
|
ENSP00000419868.1:n.*663T>G
|
|
ENST00000489173.1:n.1594T>G
|
|
|
NM_001144951.1:c.*419T>G
|
NP_001138423.1:n.*419T>G
|
|
NM_145262.3:c.1300T>G
|
NP_660305.2:p.Leu434Val
|
|
NR_026699.1:n.1398T>G
|
|
|
NR_026700.1:n.696-192T>G
|
|
|
NR_026701.1:n.1396T>G
|
|
|
NR_026702.1:n.626-192T>G
|
|
|
XM_005264878.2:c.*419T>G
|
XP_005264935.1:n.*419T>G
|
|
XR_245095.2:n.2743-192T>G
|
|
|
XM_017005730.1:c.919T>G
|
XP_016861219.1:p.Leu307Val
|
|
XM_024453351.1:c.1300T>G
|
XP_024309119.1:p.Leu434Val
|
|
XM_024453352.1:c.*419T>G
|
XP_024309120.1:n.*419T>G
|
|
XR_001740022.2:n.3202T>G
|
|
|
XR_001740023.2:n.2918-192T>G
|
|
|
XR_245095.4:n.2744-192T>G
|
|
|
NM_145262.4:c.1300T>G
MANE Select
|
NP_660305.2:p.Leu434Val
|
|
NR_026699.2:n.1390T>G
|
|
|
NR_026700.2:n.688-192T>G
|
|
|
NR_026701.2:n.1388T>G
|
|
|
NR_026702.2:n.618-192T>G
|
|
|
NM_001144951.2:c.*419T>G
|
NP_001138423.1:n.*419T>G
|
|