|
ENST00000331710.10:c.2138+2T>C
MANE Select
|
ENSP00000329967.5:n.2138+2T>C
|
|
|
ENST00000545392.2:n.1044+2T>C
|
|
|
|
ENST00000650708.1:c.2175+2T>C
|
|
|
|
ENST00000650762.1:c.1880+2T>C
|
ENSP00000498758.1:n.1880+2T>C
|
|
|
ENST00000650786.1:c.*2283+2T>C
|
ENSP00000498280.1:n.*2283+2T>C
|
|
|
ENST00000650790.1:c.2138+2T>C
|
ENSP00000498995.1:n.2138+2T>C
|
|
|
ENST00000650997.1:c.2138+2T>C
|
ENSP00000498341.1:n.2138+2T>C
|
|
|
ENST00000651014.1:c.1982+2T>C
|
ENSP00000498885.1:n.1982+2T>C
|
|
|
ENST00000651262.1:c.*405+2T>C
|
ENSP00000498461.1:n.*405+2T>C
|
|
|
ENST00000651878.1:c.*1622+2T>C
|
ENSP00000499077.1:n.*1622+2T>C
|
|
|
ENST00000652537.1:c.*518+2T>C
|
ENSP00000499102.1:n.*518+2T>C
|
|
|
ENST00000652657.1:c.2066+287T>C
|
ENSP00000498887.1:n.2066+287T>C
|
|
|
ENST00000676587.1:c.80-3289T>C
|
|
|
|
ENST00000676593.1:c.72+2T>C
|
|
|
|
ENST00000676654.1:n.2480+2T>C
|
|
|
|
ENST00000676684.1:n.2858+2T>C
|
|
|
|
ENST00000676809.1:c.*827+2T>C
|
ENSP00000504298.1:n.*827+2T>C
|
|
|
ENST00000676912.1:c.1982+2T>C
|
ENSP00000503567.1:n.1982+2T>C
|
|
|
ENST00000676930.1:c.1790+2T>C
|
ENSP00000502899.1:n.1790+2T>C
|
|
|
ENST00000677313.1:c.72+2T>C
|
|
|
|
ENST00000677499.1:c.*514+2T>C
|
ENSP00000502875.1:n.*514+2T>C
|
|
|
ENST00000677632.1:c.2123+2T>C
|
ENSP00000504586.1:n.2123+2T>C
|
|
|
ENST00000677641.1:c.2135+2T>C
|
ENSP00000504637.1:n.2135+2T>C
|
|
|
ENST00000677686.1:n.5207+2T>C
|
|
|
|
ENST00000677831.1:c.*518+2T>C
|
ENSP00000503760.1:n.*518+2T>C
|
|
|
ENST00000678180.1:c.2036+2T>C
|
ENSP00000504132.1:n.2036+2T>C
|
|
|
ENST00000678197.1:n.2121+2T>C
|
|
|
|
ENST00000331710.9:c.2138+2T>C
|
ENSP00000329967.5:n.2138+2T>C
|
|
|
NM_013254.3:c.2138+2T>C
|
NP_037386.1:n.2138+2T>C
|
|
|
XM_005268809.1:c.2138+2T>C
|
XP_005268866.1:n.2138+2T>C
|
|
|
XM_005268810.1:c.2138+2T>C
|
XP_005268867.1:n.2138+2T>C
|
|
|
XR_001748674.2:n.2360+2T>C
|
|
|
|
NM_013254.4:c.2138+2T>C
MANE Select
|
NP_037386.1:n.2138+2T>C
|
|
