ENST00000411641.7:c.573+521C>G
MANE Select
|
ENSP00000393887.2:n.573+521C>G
|
|
ENST00000273784.5:c.576+521C>G
|
ENSP00000273784.5:n.576+521C>G
|
|
ENST00000411641.6:c.573+521C>G
|
ENSP00000393887.2:n.573+521C>G
|
|
ENST00000478441.1:n.1151C>G
|
|
|
NM_001622.2:c.573+521C>G
|
NP_001613.2:n.573+521C>G
|
|
NM_001354571.1:c.576+521C>G
|
NP_001341500.1:n.576+521C>G
|
|
NM_001354572.1:c.570+521C>G
|
NP_001341501.1:n.570+521C>G
|
|
NM_001354573.1:c.573+521C>G
|
NP_001341502.1:n.573+521C>G
|
|
NM_001622.3:c.573+521C>G
|
NP_001613.2:n.573+521C>G
|
|
NM_001622.4:c.573+521C>G
MANE Select
|
NP_001613.2:n.573+521C>G
|
|
NM_001354571.2:c.576+521C>G
|
NP_001341500.1:n.576+521C>G
|
|
NM_001354572.2:c.570+521C>G
|
NP_001341501.1:n.570+521C>G
|
|
NM_001354573.2:c.573+521C>G
|
NP_001341502.1:n.573+521C>G
|
|