|
NM_001361.5:c.518-11G>A
MANE Select
|
NP_001352.2:n.518-11G>A
|
|
ENST00000219240.9:c.518-11G>A
MANE Select
|
ENSP00000219240.4:n.518-11G>A
|
|
NM_001361.4:c.518-11G>A
|
NP_001352.2:n.518-11G>A
|
|
ENST00000219240.8:c.518-11G>A
|
ENSP00000219240.4:n.518-11G>A
|
|
ENST00000571392.1:n.1485-2052G>A
|
|
|
ENST00000572003.5:n.435-11G>A
|
|
|
ENST00000572887.5:c.518-11G>A
|
ENSP00000461848.1:n.518-11G>A
|
|
ENST00000573843.1:n.481-11G>A
|
|
|
ENST00000573922.5:n.314-2052G>A
|
|
|
ENST00000574309.5:c.514-3032G>A
|
|
|
XM_005255827.2:c.434-11G>A
|
XP_005255884.1:n.434-11G>A
|
|
XM_005255827.4:c.434-11G>A
|
XP_005255884.1:n.434-11G>A
|
|
XM_005255828.3:c.110-11G>A
|
XP_005255885.1:n.110-11G>A
|
|
XM_005255829.2:c.89-11G>A
|
XP_005255886.1:n.89-11G>A
|
|
XM_005255829.4:c.89-11G>A
|
XP_005255886.1:n.89-11G>A
|
|
XM_017022990.2:c.191-11G>A
|
XP_016878479.1:n.191-11G>A
|