|
ENST00000534772.2:c.*1787-33G>T
|
ENSP00000461912.2:n.*1787-33G>T
|
|
|
ENST00000703106.1:c.1723G>T
|
ENSP00000515173.1:p.Ala575Ser
|
|
|
ENST00000703107.1:c.*1640-33G>T
|
ENSP00000515174.1:n.*1640-33G>T
|
|
|
ENST00000703108.1:c.*159-33G>T
|
ENSP00000515175.1:n.*159-33G>T
|
|
|
ENST00000703109.1:c.1744-33G>T
|
ENSP00000515176.1:n.1744-33G>T
|
|
|
ENST00000703110.1:c.*1213-33G>T
|
ENSP00000515177.1:n.*1213-33G>T
|
|
|
ENST00000703111.1:n.1718-33G>T
|
|
|
|
ENST00000703112.1:n.2484-33G>T
|
|
|
|
ENST00000703113.1:c.*1124-33G>T
|
ENSP00000515178.1:n.*1124-33G>T
|
|
|
ENST00000703114.1:c.*360-33G>T
|
ENSP00000515179.1:n.*360-33G>T
|
|
|
ENST00000703115.1:c.824-33G>T
|
ENSP00000515180.1:n.824-33G>T
|
|
|
ENST00000323786.10:c.1711-33G>T
MANE Select
|
ENSP00000315775.5:n.1711-33G>T
|
|
|
ENST00000564415.6:c.*1491-33G>T
|
ENSP00000456653.2:n.*1491-33G>T
|
|
|
ENST00000674443.1:c.1636-33G>T
|
ENSP00000501405.1:n.1636-33G>T
|
|
|
ENST00000323786.9:c.1711-33G>T
|
ENSP00000315775.5:n.1711-33G>T
|
|
|
ENST00000393612.8:c.1648-33G>T
|
ENSP00000377236.5:n.1648-33G>T
|
|
|
ENST00000482252.5:c.1858-33G>T
|
ENSP00000432802.1:n.1858-33G>T
|
|
|
ENST00000526700.5:n.887-33G>T
|
|
|
|
ENST00000530314.5:n.2390-33G>T
|
|
|
|
ENST00000564315.1:n.171-33G>T
|
|
|
|
ENST00000564415.5:c.*1491-33G>T
|
ENSP00000456653.1:n.*1491-33G>T
|
|
|
NM_001195139.1:c.1648-33G>T
|
NP_001182068.1:n.1648-33G>T
|
|
|
NM_015386.2:c.1711-33G>T
|
NP_056201.2:n.1711-33G>T
|
|
|
XM_011522981.1:c.1285-33G>T
|
XP_011521283.1:n.1285-33G>T
|
|
|
XR_933266.1:n.1657-33G>T
|
|
|
|
XR_933267.1:n.1657-33G>T
|
|
|
|
XM_011522981.3:c.1285-33G>T
|
XP_011521283.1:n.1285-33G>T
|
|
|
XM_024450224.1:c.730-33G>T
|
XP_024305992.1:n.730-33G>T
|
|
|
XR_001751889.1:n.1594-33G>T
|
|
|
|
XR_933266.2:n.1657-33G>T
|
|
|
|
NM_015386.3:c.1711-33G>T
MANE Select
|
NP_056201.2:n.1711-33G>T
|
|
|
NM_001195139.2:c.1636-33G>T
|
NP_001182068.2:n.1636-33G>T
|
|
|
NM_001365426.1:c.1285-33G>T
|
NP_001352355.1:n.1285-33G>T
|
|
|
NR_158212.1:n.1670-33G>T
|
|
|
