ENST00000602382.6:c.873-1G>C
|
ENSP00000473313.2:n.873-1G>C
|
|
ENST00000602780.2:n.2212-1G>C
|
|
|
ENST00000602860.6:n.2127-1G>C
|
|
|
ENST00000695641.1:n.2316-1G>C
|
|
|
ENST00000695648.1:c.1189-1G>C
|
ENSP00000512081.1:n.1189-1G>C
|
|
ENST00000695656.1:n.2166G>C
|
|
|
ENST00000695657.1:n.1525-1G>C
|
|
|
ENST00000695658.1:c.1030-1G>C
|
ENSP00000512088.1:n.1030-1G>C
|
|
ENST00000695659.1:c.1224G>C
|
ENSP00000512089.1:p.Gln408His
|
|
ENST00000695662.1:c.*686-1G>C
|
ENSP00000512091.1:n.*686-1G>C
|
|
ENST00000695694.1:c.1162-1G>C
|
ENSP00000512105.1:n.1162-1G>C
|
|
ENST00000695695.1:n.1273-1G>C
|
|
|
ENST00000695696.1:n.1254-1G>C
|
|
|
ENST00000695697.1:c.1120-1G>C
|
ENSP00000512106.1:n.1120-1G>C
|
|
ENST00000695698.1:n.1457-1G>C
|
|
|
ENST00000695699.1:n.1626G>C
|
|
|
ENST00000695709.1:n.482-1G>C
|
|
|
ENST00000695710.1:n.1841-1G>C
|
|
|
ENST00000695711.1:c.*515-1G>C
|
ENSP00000512109.1:n.*515-1G>C
|
|
ENST00000695712.1:c.*957-1G>C
|
ENSP00000512110.1:n.*957-1G>C
|
|
ENST00000695731.1:c.530-1G>C
|
|
|
ENST00000695732.1:c.646-1G>C
|
ENSP00000512125.1:n.646-1G>C
|
|
ENST00000695733.1:c.786-1G>C
|
ENSP00000512126.1:n.786-1G>C
|
|
ENST00000695734.1:c.1207-1G>C
|
ENSP00000512127.1:n.1207-1G>C
|
|
ENST00000219251.13:c.1198-1G>C
|
ENSP00000219251.8:n.1198-1G>C
|
|
ENST00000620761.6:c.1207-1G>C
MANE Select
|
ENSP00000478084.1:n.1207-1G>C
|
|
ENST00000219251.12:c.1456-1G>C
|
ENSP00000219251.7:n.1456-1G>C
|
|
ENST00000393919.8:c.1465-1G>C
|
ENSP00000377496.4:n.1465-1G>C
|
|
ENST00000602320.1:c.1198-40G>C
|
ENSP00000473679.2:n.1198-40G>C
|
|
ENST00000602382.5:c.415-1G>C
|
|
|
ENST00000602622.5:n.2206-1G>C
|
|
|
ENST00000602656.1:n.470G>C
|
|
|
ENST00000602860.5:n.1645-1G>C
|
|
|
ENST00000620338.4:c.1465-1G>C
|
ENSP00000483117.1:n.1465-1G>C
|
|
ENST00000620761.4:c.1207-1G>C
|
ENSP00000478084.1:n.1207-1G>C
|
|
NM_001082486.1:c.1465-1G>C
|
NP_001075955.1:n.1465-1G>C
|
|
NM_001082487.1:c.1456-40G>C
|
NP_001075956.1:n.1456-40G>C
|
|
NM_022914.2:c.1456-1G>C
|
NP_075065.2:n.1456-1G>C
|
|
XM_005256115.2:c.1378-1G>C
|
XP_005256172.1:n.1378-1G>C
|
|
NM_001082486.2:c.1207-1G>C
MANE Select
|
NP_001075955.2:n.1207-1G>C
|
|
NM_022914.3:c.1198-1G>C
|
NP_075065.3:n.1198-1G>C
|
|
XM_005256115.4:c.1378-1G>C
|
XP_005256172.1:n.1378-1G>C
|
|