ENST00000327047.6:c.*1332G>C
MANE Select
|
ENSP00000322280.1:n.*1332G>C
|
|
ENST00000295911.6:c.*248G>C
|
ENSP00000295911.2:n.*248G>C
|
|
ENST00000327047.5:c.*1332G>C
|
ENSP00000322280.1:n.*1332G>C
|
|
ENST00000562308.5:c.104+14978G>C
|
|
|
ENST00000565169.1:c.162+14978G>C
|
|
|
ENST00000569170.5:c.162+14978G>C
|
|
|
NM_001195794.1:c.*1332G>C , LRG_700t1:c.*1332G>C
|
NP_001182723.1:n.*1332G>C
|
|
NM_001256819.1:c.*1645G>C
|
NP_001243748.1:n.*1645G>C
|
|
NM_052995.2:c.*248G>C , LRG_700t2:c.*248G>C
|
NP_443721.1:n.*248G>C
|
|
NM_174878.2:c.*1332G>C
|
NP_777367.1:n.*1332G>C
|
|
NR_046380.2:n.2512G>C
|
|
|
XR_924167.1:n.2343G>C
|
|
|
NM_001256819.2:c.*1645G>C
|
NP_001243748.1:n.*1645G>C
|
|
NM_174878.3:c.*1332G>C
MANE Select
|
NP_777367.1:n.*1332G>C
|
|
NR_046380.3:n.2240G>C
|
|
|