ENST00000474381.2:n.3059+27T>G
|
|
|
ENST00000481849.6:n.2605T>G
|
|
|
ENST00000497377.6:n.2512T>G
|
|
|
ENST00000640094.2:c.895+237T>G
|
ENSP00000491275.2:n.895+237T>G
|
|
ENST00000696558.1:c.1081+27T>G
|
ENSP00000512716.1:n.1081+27T>G
|
|
ENST00000696559.1:c.1012+27T>G
|
ENSP00000512717.1:n.1012+27T>G
|
|
ENST00000696560.1:c.1012+27T>G
|
ENSP00000512718.1:n.1012+27T>G
|
|
ENST00000696561.1:c.1012+27T>G
|
ENSP00000512719.1:n.1012+27T>G
|
|
ENST00000696562.1:c.1012+27T>G
|
ENSP00000512720.1:n.1012+27T>G
|
|
ENST00000412585.7:c.1012+27T>G
MANE Select
|
ENSP00000399168.2:n.1012+27T>G
|
|
ENST00000640094.1:c.88+237T>G
|
ENSP00000491275.1:n.88+237T>G
|
|
ENST00000412585.6:c.1012+27T>G
|
ENSP00000399168.2:n.1012+27T>G
|
|
NM_005514.6:c.1012+27T>G
|
NP_005505.2:n.1012+27T>G
|
|
XM_011514556.1:c.1045+27T>G
|
XP_011512858.1:n.1045+27T>G
|
|
XM_011514557.1:c.895+237T>G
|
XP_011512859.1:n.895+237T>G
|
|
XR_926175.1:n.1451+27T>G
|
|
|
NM_005514.7:c.1012+27T>G
|
NP_005505.2:n.1012+27T>G
|
|
NM_005514.8:c.1012+27T>G
MANE Select
|
NP_005505.2:n.1012+27T>G
|
|