ENST00000205402.10:c.1046+2T>G
MANE Select
|
ENSP00000205402.3:n.1046+2T>G
|
|
ENST00000205402.9:c.1046+2T>G
|
ENSP00000205402.3:n.1046+2T>G
|
|
ENST00000415325.5:c.*720+2T>G
|
ENSP00000402593.1:n.*720+2T>G
|
|
ENST00000417551.5:c.1046+2T>G
|
ENSP00000390667.1:n.1046+2T>G
|
|
ENST00000437604.6:c.902+2T>G
|
ENSP00000387542.2:n.902+2T>G
|
|
ENST00000440410.5:c.977+2T>G
|
ENSP00000417016.1:n.977+2T>G
|
|
NM_000108.4:c.1046+2T>G
|
NP_000099.2:n.1046+2T>G
|
|
NM_001289750.1:c.749+2T>G
|
NP_001276679.1:n.749+2T>G
|
|
NM_001289751.1:c.977+2T>G
|
NP_001276680.1:n.977+2T>G
|
|
NM_001289752.1:c.902+2T>G
|
NP_001276681.1:n.902+2T>G
|
|
NM_000108.5:c.1046+2T>G
MANE Select
|
NP_000099.2:n.1046+2T>G
|
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