ENST00000474381.2:n.3060-1G>T
|
|
|
ENST00000481849.6:n.3019G>T
|
|
|
ENST00000497377.6:n.2926G>T
|
|
|
ENST00000640094.2:c.896-1G>T
|
ENSP00000491275.2:n.896-1G>T
|
|
ENST00000696558.1:c.1082-1G>T
|
ENSP00000512716.1:n.1082-1G>T
|
|
ENST00000696559.1:c.1013-1G>T
|
ENSP00000512717.1:n.1013-1G>T
|
|
ENST00000696560.1:c.1013-1G>T
|
ENSP00000512718.1:n.1013-1G>T
|
|
ENST00000696561.1:c.1013-1G>T
|
ENSP00000512719.1:n.1013-1G>T
|
|
ENST00000696562.1:c.1013-1G>T
|
ENSP00000512720.1:n.1013-1G>T
|
|
ENST00000412585.7:c.1013-1G>T
MANE Select
|
ENSP00000399168.2:n.1013-1G>T
|
|
ENST00000640094.1:c.89-1G>T
|
ENSP00000491275.1:n.89-1G>T
|
|
ENST00000412585.6:c.1013-1G>T
|
ENSP00000399168.2:n.1013-1G>T
|
|
ENST00000481849.5:n.141G>T
|
|
|
ENST00000497377.5:n.411G>T
|
|
|
NM_005514.6:c.1013-1G>T
|
NP_005505.2:n.1013-1G>T
|
|
XM_011514556.1:c.1046-1G>T
|
XP_011512858.1:n.1046-1G>T
|
|
XM_011514557.1:c.896-1G>T
|
XP_011512859.1:n.896-1G>T
|
|
XR_926175.1:n.1452-1G>T
|
|
|
NM_005514.7:c.1013-1G>T
|
NP_005505.2:n.1013-1G>T
|
|
NM_005514.8:c.1013-1G>T
MANE Select
|
NP_005505.2:n.1013-1G>T
|
|