ENST00000567109.6:c.960+7742A>G
MANE Select
|
ENSP00000479395.1:n.960+7742A>G
|
|
ENST00000268613.14:c.1101+7742A>G
|
ENSP00000268613.10:n.1101+7742A>G
|
|
ENST00000428848.7:c.843+7742A>G
|
ENSP00000394557.3:n.843+7742A>G
|
|
ENST00000539548.6:c.*592+7742A>G
|
ENSP00000442225.2:n.*592+7742A>G
|
|
ENST00000566620.5:c.924+7742A>G
|
ENSP00000454435.3:n.924+7742A>G
|
|
ENST00000567109.5:c.960+7742A>G
|
ENSP00000479395.1:n.960+7742A>G
|
|
ENST00000622885.4:c.804+7742A>G
|
ENSP00000483719.1:n.804+7742A>G
|
|
NM_001220488.1:c.1101+7742A>G
|
NP_001207417.1:n.1101+7742A>G
|
|
NM_001220489.1:c.843+7742A>G
|
NP_001207418.1:n.843+7742A>G
|
|
NM_001220490.1:c.198+7742A>G
|
NP_001207419.1:n.198+7742A>G
|
|
NM_001257.4:c.960+7742A>G
|
NP_001248.1:n.960+7742A>G
|
|
XM_011522804.1:c.657+7742A>G
|
XP_011521106.1:n.657+7742A>G
|
|
XM_011522805.1:c.1101+7742A>G
|
XP_011521107.1:n.1101+7742A>G
|
|
XM_011522804.3:c.657+7742A>G
|
XP_011521106.1:n.657+7742A>G
|
|
XM_017022848.2:c.1101+7742A>G
|
XP_016878337.1:n.1101+7742A>G
|
|
NM_001257.5:c.960+7742A>G
MANE Select
|
NP_001248.1:n.960+7742A>G
|
|
NM_001220488.2:c.1101+7742A>G
|
NP_001207417.1:n.1101+7742A>G
|
|
NM_001220489.2:c.843+7742A>G
|
NP_001207418.1:n.843+7742A>G
|
|
NM_001220490.2:c.198+7742A>G
|
NP_001207419.1:n.198+7742A>G
|
|