ENST00000420013.6:c.*1658A>G
|
ENSP00000404422.2:n.*1658A>G
|
|
ENST00000453297.6:c.5204A>G
|
ENSP00000392953.2:n.5204A>G
|
|
ENST00000704386.1:c.*2139A>G
|
ENSP00000515888.1:n.*2139A>G
|
|
ENST00000535094.7:c.*1658A>G
MANE Select
|
ENSP00000440374.2:n.*1658A>G
|
|
ENST00000375604.6:c.*1658A>G
|
ENSP00000364754.3:n.*1658A>G
|
|
ENST00000397030.5:c.*2030A>G
|
ENSP00000380225.1:n.*2030A>G
|
|
ENST00000469415.1:n.2996A>G
|
|
|
ENST00000488765.1:n.3176A>G
|
|
|
NM_001112732.2:c.*1658A>G
|
NP_001106203.2:n.*1658A>G
|
|
NM_024979.4:c.*1658A>G
|
NP_079255.4:n.*1658A>G
|
|
XM_005268309.2:c.*1658A>G
|
XP_005268366.1:n.*1658A>G
|
|
XM_011537482.1:c.*1658A>G
|
XP_011535784.1:n.*1658A>G
|
|
XM_011537483.1:c.*1658A>G
|
XP_011535785.1:n.*1658A>G
|
|
XM_011537484.1:c.*1658A>G
|
XP_011535786.1:n.*1658A>G
|
|
XM_011537485.1:c.*1658A>G
|
XP_011535787.1:n.*1658A>G
|
|
XM_011537486.1:c.*1658A>G
|
XP_011535788.1:n.*1658A>G
|
|
XM_011537487.1:c.*1658A>G
|
XP_011535789.1:n.*1658A>G
|
|
XM_011537488.1:c.*1658A>G
|
XP_011535790.1:n.*1658A>G
|
|
XM_011537489.1:c.*1658A>G
|
XP_011535791.1:n.*1658A>G
|
|
XM_011537490.1:c.*1658A>G
|
XP_011535792.1:n.*1658A>G
|
|
XM_011537491.1:c.*1658A>G
|
XP_011535793.1:n.*1658A>G
|
|
NM_001320815.1:c.*1658A>G
|
NP_001307744.1:n.*1658A>G
|
|
NM_001320816.1:c.*1658A>G
|
NP_001307745.1:n.*1658A>G
|
|
NM_001366644.1:c.*1658A>G
|
NP_001353573.1:n.*1658A>G
|
|
NM_001366645.1:c.*1658A>G
|
NP_001353574.1:n.*1658A>G
|
|
NM_001366646.1:c.*1658A>G
|
NP_001353575.1:n.*1658A>G
|
|
XM_011537483.2:c.*1658A>G
|
XP_011535785.1:n.*1658A>G
|
|
XM_011537486.2:c.*1658A>G
|
XP_011535788.2:n.*1658A>G
|
|
XM_017020493.1:c.*1658A>G
|
XP_016875982.1:n.*1658A>G
|
|
XM_017020494.1:c.*1658A>G
|
XP_016875983.1:n.*1658A>G
|
|
XM_017020495.1:c.*1658A>G
|
XP_016875984.1:n.*1658A>G
|
|
NM_001112732.3:c.*1658A>G
MANE Select
|
NP_001106203.2:n.*1658A>G
|
|
NM_001320815.2:c.*1658A>G
|
NP_001307744.1:n.*1658A>G
|
|
NM_001320816.2:c.*1658A>G
|
NP_001307745.1:n.*1658A>G
|
|
NM_001366644.2:c.*1658A>G
|
NP_001353573.1:n.*1658A>G
|
|
NM_001366645.2:c.*1658A>G
|
NP_001353574.1:n.*1658A>G
|
|
NM_001366646.2:c.*1658A>G
|
NP_001353575.1:n.*1658A>G
|
|