|
ENST00000370360.8:c.1214+302C>G
MANE Select
|
ENSP00000359385.3:n.1214+302C>G
|
|
|
ENST00000370360.7:c.1214+302C>G
|
ENSP00000359385.3:n.1214+302C>G
|
|
|
ENST00000463560.1:c.562+423C>G
|
|
|
|
ENST00000495106.5:c.1214+302C>G
|
ENSP00000436829.1:n.1214+302C>G
|
|
|
ENST00000495852.6:c.437+302C>G
|
ENSP00000469157.2:n.437+302C>G
|
|
|
NM_053274.2:c.1214+302C>G
|
NP_444504.1:n.1214+302C>G
|
|
|
XM_005270400.1:c.1172+302C>G
|
XP_005270457.1:n.1172+302C>G
|
|
|
XM_005270401.2:c.1088+302C>G
|
XP_005270458.1:n.1088+302C>G
|
|
|
XM_006710309.1:c.713+302C>G
|
XP_006710372.1:n.713+302C>G
|
|
|
XM_011540544.1:c.1214+302C>G
|
XP_011538846.1:n.1214+302C>G
|
|
|
XM_011540545.1:c.1214+302C>G
|
XP_011538847.1:n.1214+302C>G
|
|
|
XM_011540546.1:c.1214+302C>G
|
XP_011538848.1:n.1214+302C>G
|
|
|
XR_946529.1:n.1309+423C>G
|
|
|
|
NM_001319683.1:c.1172+302C>G
|
NP_001306612.1:n.1172+302C>G
|
|
|
NR_135089.1:n.1329+302C>G
|
|
|
|
XM_005270401.3:c.1088+302C>G
|
XP_005270458.1:n.1088+302C>G
|
|
|
XM_006710309.2:c.713+302C>G
|
XP_006710372.1:n.713+302C>G
|
|
|
XM_011540546.2:c.1214+302C>G
|
XP_011538848.1:n.1214+302C>G
|
|
|
XM_017000137.1:c.1313+302C>G
|
XP_016855626.1:n.1313+302C>G
|
|
|
XM_017000138.1:c.1271+302C>G
|
XP_016855627.1:n.1271+302C>G
|
|
|
XM_017000139.1:c.1293+423C>G
|
XP_016855628.1:n.1293+423C>G
|
|
|
XM_017000140.1:c.1187+302C>G
|
XP_016855629.1:n.1187+302C>G
|
|
|
XM_017000141.1:c.1194+423C>G
|
XP_016855630.1:n.1194+423C>G
|
|
|
XM_017000142.1:c.671+302C>G
|
XP_016855631.1:n.671+302C>G
|
|
|
XM_017000143.1:c.671+302C>G
|
XP_016855632.1:n.671+302C>G
|
|
|
XM_017000144.1:c.443+302C>G
|
XP_016855633.1:n.443+302C>G
|
|
|
XR_002959248.1:n.1677+423C>G
|
|
|
|
XR_002959249.1:n.1309+423C>G
|
|
|
|
NM_053274.3:c.1214+302C>G
MANE Select
|
NP_444504.1:n.1214+302C>G
|
|
|
NM_001319683.2:c.1172+302C>G
|
NP_001306612.1:n.1172+302C>G
|
|
|
NR_135089.2:n.1307+302C>G
|
|
|
