ENST00000389266.8:c.1699+287G>C
MANE Select
|
ENSP00000373918.3:n.1699+287G>C
|
|
ENST00000444666.6:c.1699+287G>C
|
ENSP00000415447.2:n.1699+287G>C
|
|
ENST00000470392.2:n.1789+287G>C
|
|
|
ENST00000485784.2:n.1778+287G>C
|
|
|
ENST00000674616.1:c.*1413+287G>C
|
ENSP00000502408.1:n.*1413+287G>C
|
|
ENST00000674643.1:c.*799+287G>C
|
ENSP00000501636.1:n.*799+287G>C
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|
ENST00000674737.1:c.*1037+287G>C
|
ENSP00000502464.1:n.*1037+287G>C
|
|
ENST00000674807.1:c.1614-1954G>C
|
ENSP00000502814.1:n.1614-1954G>C
|
|
ENST00000674815.1:c.1330+287G>C
|
ENSP00000502799.1:n.1330+287G>C
|
|
ENST00000674851.1:c.1330+287G>C
|
ENSP00000502451.1:n.1330+287G>C
|
|
ENST00000674969.1:n.3572+287G>C
|
|
|
ENST00000675051.1:c.1498+287G>C
|
ENSP00000502296.1:n.1498+287G>C
|
|
ENST00000675529.1:c.*1569+287G>C
|
ENSP00000501655.1:n.*1569+287G>C
|
|
ENST00000675587.1:n.2531+287G>C
|
|
|
ENST00000675651.1:c.1699+287G>C
|
ENSP00000502513.1:n.1699+287G>C
|
|
ENST00000675693.1:c.1531+287G>C
|
ENSP00000502174.1:n.1531+287G>C
|
|
ENST00000675810.1:c.1597+287G>C
|
ENSP00000502743.1:n.1597+287G>C
|
|
ENST00000675859.1:c.1614-1954G>C
|
ENSP00000502033.1:n.1614-1954G>C
|
|
ENST00000675863.1:n.1707+287G>C
|
|
|
ENST00000675886.1:n.7739+287G>C
|
|
|
ENST00000676088.1:c.*1641+287G>C
|
ENSP00000501884.1:n.*1641+287G>C
|
|
ENST00000676140.1:c.*644+287G>C
|
ENSP00000502571.1:n.*644+287G>C
|
|
ENST00000676164.1:c.*1150+287G>C
|
ENSP00000501986.1:n.*1150+287G>C
|
|
ENST00000676210.1:c.*988+287G>C
|
ENSP00000502373.1:n.*988+287G>C
|
|
ENST00000676259.1:c.*1131+287G>C
|
ENSP00000501980.1:n.*1131+287G>C
|
|
ENST00000676403.1:c.1699+287G>C
|
ENSP00000502681.1:n.1699+287G>C
|
|
ENST00000389266.7:c.1699+287G>C
|
ENSP00000373918.3:n.1699+287G>C
|
|
ENST00000444666.5:c.220+287G>C
|
ENSP00000415447.1:n.220+287G>C
|
|
ENST00000470392.1:n.421+287G>C
|
|
|
NM_001316772.1:c.1537+287G>C
|
NP_001303701.1:n.1537+287G>C
|
|
NM_002047.2:c.1699+287G>C , LRG_243t1:c.1699+287G>C
|
NP_002038.2:n.1699+287G>C
|
|
NM_002047.3:c.1699+287G>C
|
NP_002038.2:n.1699+287G>C
|
|
XM_006715686.1:c.1330+287G>C
|
XP_006715749.1:n.1330+287G>C
|
|
XM_006715686.2:c.1330+287G>C
|
XP_006715749.1:n.1330+287G>C
|
|
NM_002047.4:c.1699+287G>C
MANE Select
|
NP_002038.2:n.1699+287G>C
|
|