ENST00000534751.3:c.554+1238C>T
|
ENSP00000456942.2:n.554+1238C>T
|
|
ENST00000683152.1:c.554+1238C>T
MANE Select
|
ENSP00000507575.1:n.554+1238C>T
|
|
ENST00000622142.5:c.554+1238C>T
|
ENSP00000480626.1:n.554+1238C>T
|
|
ENST00000424263.6:c.554+1238C>T
|
ENSP00000394314.2:n.554+1238C>T
|
|
ENST00000528980.1:n.275+1238C>T
|
|
|
ENST00000530656.5:c.656+1238C>T
|
ENSP00000435976.1:n.656+1238C>T
|
|
ENST00000534751.2:c.444+1238C>T
|
|
|
ENST00000622142.4:c.554+1238C>T
|
ENSP00000480626.1:n.554+1238C>T
|
|
NM_001256695.1:c.554+1238C>T
|
NP_001243624.1:n.554+1238C>T
|
|
NM_001256696.1:c.554+1238C>T
|
NP_001243625.1:n.554+1238C>T
|
|
NR_046338.1:n.905+1238C>T
|
|
|
XM_011520222.1:c.554+1238C>T
|
XP_011518524.1:n.554+1238C>T
|
|
XM_011520223.1:c.554+1238C>T
|
XP_011518525.1:n.554+1238C>T
|
|
XM_011520224.1:c.554+1238C>T
|
XP_011518526.1:n.554+1238C>T
|
|
XM_011520225.1:c.554+1238C>T
|
XP_011518527.1:n.554+1238C>T
|
|
XM_011520226.1:c.5+1238C>T
|
XP_011518528.1:n.5+1238C>T
|
|
XM_011520227.1:c.5+1238C>T
|
XP_011518529.1:n.5+1238C>T
|
|
XM_011520228.1:c.554+1238C>T
|
XP_011518530.1:n.554+1238C>T
|
|
XM_011520229.1:c.-12+1238C>T
|
XP_011518531.1:n.-12+1238C>T
|
|
XM_011520230.1:c.554+1238C>T
|
XP_011518532.1:n.554+1238C>T
|
|
XM_011520231.1:c.554+1238C>T
|
XP_011518533.1:n.554+1238C>T
|
|
XR_930882.1:n.985+1238C>T
|
|
|
NM_001359633.1:c.656+1238C>T
|
NP_001346562.1:n.656+1238C>T
|
|
XM_011520222.2:c.554+1238C>T
|
XP_011518524.1:n.554+1238C>T
|
|
XM_011520223.2:c.554+1238C>T
|
XP_011518525.1:n.554+1238C>T
|
|
XM_011520224.3:c.554+1238C>T
|
XP_011518526.1:n.554+1238C>T
|
|
XM_011520225.2:c.554+1238C>T
|
XP_011518527.1:n.554+1238C>T
|
|
XM_011520226.2:c.5+1238C>T
|
XP_011518528.1:n.5+1238C>T
|
|
XM_011520227.2:c.5+1238C>T
|
XP_011518529.1:n.5+1238C>T
|
|
XM_011520228.3:c.554+1238C>T
|
XP_011518530.1:n.554+1238C>T
|
|
NM_001256695.2:c.554+1238C>T
|
NP_001243624.1:n.554+1238C>T
|
|
NM_001256696.2:c.554+1238C>T
|
NP_001243625.1:n.554+1238C>T
|
|
NM_001359633.2:c.554+1238C>T
|
NP_001346562.2:n.554+1238C>T
|
|
NM_001384648.1:c.554+1238C>T
MANE Select
|
NP_001371577.1:n.554+1238C>T
|
|
NM_001384649.1:c.554+1238C>T
|
NP_001371578.1:n.554+1238C>T
|
|
NM_001384650.1:c.554+1238C>T
|
NP_001371579.1:n.554+1238C>T
|
|
NM_001384651.1:c.554+1238C>T
|
NP_001371580.1:n.554+1238C>T
|
|