ENST00000478003.2:n.2814G>A
|
|
|
ENST00000682103.1:c.526+1G>A
|
|
|
ENST00000682276.1:n.2430+1G>A
|
|
|
ENST00000682468.1:n.523+1G>A
|
|
|
ENST00000682603.1:c.217+1G>A
|
|
|
ENST00000682844.1:c.41+1G>A
|
|
|
ENST00000682892.1:c.2532+1G>A
|
ENSP00000507214.1:n.2532+1G>A
|
|
ENST00000682952.1:n.2624+1G>A
|
|
|
ENST00000684455.1:c.2198+1G>A
|
|
|
ENST00000684642.1:c.2214+3793G>A
|
ENSP00000507355.1:n.2214+3793G>A
|
|
ENST00000684740.1:n.3163+1G>A
|
|
|
ENST00000303236.9:c.2985+1G>A
MANE Select
|
ENSP00000307235.3:n.2985+1G>A
|
|
ENST00000652099.1:c.3179+1G>A
|
|
|
ENST00000652736.1:n.2861+1G>A
|
|
|
ENST00000303236.7:c.2985+1G>A
|
ENSP00000307235.3:n.2985+1G>A
|
|
ENST00000415570.1:c.2622+1G>A
|
ENSP00000412076.1:n.2622+1G>A
|
|
ENST00000419748.5:c.2532+1G>A
|
ENSP00000408325.1:n.2532+1G>A
|
|
NM_001313915.1:c.2532+1G>A
|
NP_001300844.1:n.2532+1G>A
|
|
NM_004836.5:c.2985+1G>A
|
NP_004827.4:n.2985+1G>A
|
|
NM_004836.6:c.2985+1G>A
|
NP_004827.4:n.2985+1G>A
|
|
NR_110236.1:n.651-3641C>T
|
|
|
XM_005264649.3:c.2301+1G>A
|
XP_005264706.1:n.2301+1G>A
|
|
XM_017005376.2:c.2301+1G>A
|
XP_016860865.1:n.2301+1G>A
|
|
NM_004836.7:c.2985+1G>A
MANE Select
|
NP_004827.4:n.2985+1G>A
|
|
NM_001313915.2:c.2532+1G>A
|
NP_001300844.1:n.2532+1G>A
|
|