ENST00000700065.1:n.759+9911G>T
|
|
|
ENST00000700066.1:c.263+9911G>T
|
ENSP00000514780.1:n.263+9911G>T
|
|
ENST00000700067.1:n.761+9911G>T
|
|
|
ENST00000700068.1:n.761+9911G>T
|
|
|
ENST00000700069.1:c.746+9911G>T
|
ENSP00000514781.1:n.746+9911G>T
|
|
ENST00000700070.1:c.*405+9911G>T
|
ENSP00000514782.1:n.*405+9911G>T
|
|
ENST00000700071.1:n.777-9401G>T
|
|
|
ENST00000281513.10:c.746+9911G>T
MANE Select
|
ENSP00000281513.5:n.746+9911G>T
|
|
ENST00000281513.9:c.746+9911G>T
|
ENSP00000281513.5:n.746+9911G>T
|
|
NM_015909.3:c.746+9911G>T
|
NP_056993.2:n.746+9911G>T
|
|
NR_052013.2:n.790+9911G>T
|
|
|
XM_011510357.1:c.746+9911G>T
|
XP_011508659.1:n.746+9911G>T
|
|
XM_011510358.1:c.746+9911G>T
|
XP_011508660.1:n.746+9911G>T
|
|
XM_011510359.1:c.107+9911G>T
|
XP_011508661.1:n.107+9911G>T
|
|
XM_011510357.2:c.746+9911G>T
|
XP_011508659.1:n.746+9911G>T
|
|
XM_011510358.2:c.746+9911G>T
|
XP_011508660.1:n.746+9911G>T
|
|
XM_017004317.1:c.746+9911G>T
|
XP_016859806.1:n.746+9911G>T
|
|
XM_024452961.1:c.107+9911G>T
|
XP_024308729.1:n.107+9911G>T
|
|
NM_015909.4:c.746+9911G>T
MANE Select
|
NP_056993.2:n.746+9911G>T
|
|
NR_052013.3:n.776+9911G>T
|
|
|