ENST00000260356.6:c.-30+47T>G
MANE Select
|
ENSP00000260356.5:n.-30+47T>G
|
|
ENST00000260356.5:c.-30+47T>G
|
ENSP00000260356.5:n.-30+47T>G
|
|
ENST00000397591.2:c.-151+47T>G
|
ENSP00000380720.2:n.-151+47T>G
|
|
NM_003246.2:c.-30+47T>G
|
NP_003237.2:n.-30+47T>G
|
|
NM_003246.3:c.-30+47T>G
|
NP_003237.2:n.-30+47T>G
|
|
XM_011521970.1:c.-151+47T>G
|
XP_011520272.1:n.-151+47T>G
|
|
XM_011521971.1:c.-30+47T>G
|
XP_011520273.1:n.-30+47T>G
|
|
XR_931897.1:n.146+47T>G
|
|
|
XM_011521971.2:c.-30+47T>G
|
XP_011520273.1:n.-30+47T>G
|
|
NM_003246.4:c.-30+47T>G
MANE Select
|
NP_003237.2:n.-30+47T>G
|
|