ENST00000615310.5:c.1983del
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ENSP00000480088.2:p.Cys662AlafsTer?
|
|
ENST00000683007.1:n.1953del
|
|
|
ENST00000683872.1:n.1944del
|
|
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ENST00000340058.6:c.2379del
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ENSP00000344798.4:p.Cys794AlafsTer?
|
|
ENST00000355710.8:c.2379del
MANE Select
|
ENSP00000347942.3:p.Cys794AlafsTer?
|
|
ENST00000671844.1:c.*973del
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ENSP00000500541.1:n.*973del
|
|
ENST00000672389.1:c.*973del
|
ENSP00000500252.1:n.*973del
|
|
ENST00000340058.5:c.2379del
|
ENSP00000344798.4:p.Cys794AlafsTer?
|
|
ENST00000355710.7:c.2379del
|
ENSP00000347942.3:p.Cys794AlafsTer?
|
|
ENST00000615310.4:c.1290-1235del
|
ENSP00000480088.1:n.1290-1235del
|
|
NM_020630.4:c.2379del , LRG_518t2:c.2379del
|
NP_065681.1:p.Cys794AlafsTer?
|
|
NM_020975.4:c.2379del , LRG_518t1:c.2379del
|
NP_066124.1:p.Cys794AlafsTer?
|
|
XM_011540027.1:c.2379del
|
XP_011538329.1:p.Cys794AlafsTer?
|
|
NM_001355216.1:c.1617del
|
NP_001342145.1:p.Cys540AlafsTer?
|
|
NM_020630.5:c.2379del
|
NP_065681.1:p.Cys794AlafsTer?
|
|
NM_020975.5:c.2379del
|
NP_066124.1:p.Cys794AlafsTer?
|
|
NM_020975.6:c.2379del
MANE Select
|
NP_066124.1:p.Cys794AlafsTer?
|
|
NM_020630.6:c.2379del
|
NP_065681.1:p.Cys794AlafsTer?
|
|