ENST00000327047.6:c.*1204G>T
MANE Select
|
ENSP00000322280.1:n.*1204G>T
|
|
ENST00000295911.6:c.*120G>T
|
ENSP00000295911.2:n.*120G>T
|
|
ENST00000327047.5:c.*1204G>T
|
ENSP00000322280.1:n.*1204G>T
|
|
ENST00000562308.5:c.104+14850G>T
|
|
|
ENST00000565169.1:c.162+14850G>T
|
|
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ENST00000569170.5:c.162+14850G>T
|
|
|
NM_001195794.1:c.*1204G>T , LRG_700t1:c.*1204G>T
|
NP_001182723.1:n.*1204G>T
|
|
NM_001256819.1:c.*1517G>T
|
NP_001243748.1:n.*1517G>T
|
|
NM_052995.2:c.*120G>T , LRG_700t2:c.*120G>T
|
NP_443721.1:n.*120G>T
|
|
NM_174878.2:c.*1204G>T
|
NP_777367.1:n.*1204G>T
|
|
NR_046380.2:n.2384G>T
|
|
|
XR_924167.1:n.2215G>T
|
|
|
NM_001256819.2:c.*1517G>T
|
NP_001243748.1:n.*1517G>T
|
|
NM_174878.3:c.*1204G>T
MANE Select
|
NP_777367.1:n.*1204G>T
|
|
NR_046380.3:n.2112G>T
|
|
|