ENST00000338376.8:c.971+193T>C
MANE Select
|
ENSP00000342493.3:n.971+193T>C
|
|
ENST00000260385.10:c.971+193T>C
|
ENSP00000260385.6:n.971+193T>C
|
|
ENST00000338376.7:c.971+193T>C
|
ENSP00000342493.3:n.971+193T>C
|
|
ENST00000558232.5:c.477+193T>C
|
|
|
ENST00000558560.1:n.478-1898T>C
|
|
|
ENST00000558777.5:c.*522+193T>C
|
ENSP00000453357.1:n.*522+193T>C
|
|
ENST00000560460.5:c.686+193T>C
|
ENSP00000453978.1:n.686+193T>C
|
|
ENST00000560779.5:n.320+193T>C
|
|
|
NM_001304802.1:c.971+193T>C
|
NP_001291731.1:n.971+193T>C
|
|
NM_018145.2:c.971+193T>C
|
NP_060615.1:n.971+193T>C
|
|
XM_005254531.1:c.971+193T>C
|
XP_005254588.1:n.971+193T>C
|
|
XM_011521755.1:c.353+193T>C
|
XP_011520057.1:n.353+193T>C
|
|
NM_001323894.1:c.971+193T>C
|
NP_001310823.1:n.971+193T>C
|
|
NM_001323895.1:c.584+193T>C
|
NP_001310824.1:n.584+193T>C
|
|
NM_001323896.1:c.1049+193T>C
|
NP_001310825.1:n.1049+193T>C
|
|
NM_001323897.1:c.1049+193T>C
|
NP_001310826.1:n.1049+193T>C
|
|
XM_011521755.2:c.353+193T>C
|
XP_011520057.1:n.353+193T>C
|
|
NM_018145.3:c.971+193T>C
MANE Select
|
NP_060615.1:n.971+193T>C
|
|
NM_001304802.2:c.971+193T>C
|
NP_001291731.1:n.971+193T>C
|
|
NM_001323894.2:c.971+193T>C
|
NP_001310823.1:n.971+193T>C
|
|
NM_001323895.2:c.584+193T>C
|
NP_001310824.1:n.584+193T>C
|
|
NM_001323896.2:c.1049+193T>C
|
NP_001310825.1:n.1049+193T>C
|
|
NM_001323897.2:c.1049+193T>C
|
NP_001310826.1:n.1049+193T>C
|
|