|
ENST00000478723.6:n.201-1G>C
|
|
|
|
ENST00000482363.2:n.1296G>C
|
|
|
|
ENST00000485675.2:n.1290G>C
|
|
|
|
ENST00000688055.1:c.130-1G>C
|
ENSP00000508688.1:n.130-1G>C
|
|
|
ENST00000382564.8:c.130-1G>C
MANE Select
|
ENSP00000372005.2:n.130-1G>C
|
|
|
ENST00000643241.1:c.55-1G>C
|
ENSP00000496401.1:n.55-1G>C
|
|
|
ENST00000646965.1:c.-46-1027G>C
|
ENSP00000496456.1:n.-46-1027G>C
|
|
|
ENST00000382564.6:c.130-1G>C
|
ENSP00000372005.2:n.130-1G>C
|
|
|
ENST00000469657.5:c.129+1000G>C
|
ENSP00000418058.1:n.129+1000G>C
|
|
|
ENST00000478723.5:n.269-1G>C
|
|
|
|
ENST00000479269.5:c.55-1G>C
|
ENSP00000419191.1:n.55-1G>C
|
|
|
ENST00000485675.1:n.1202G>C
|
|
|
|
ENST00000486355.1:c.130-1G>C
|
ENSP00000419991.1:n.130-1G>C
|
|
|
ENST00000491873.5:c.55-1G>C
|
ENSP00000420767.1:n.55-1G>C
|
|
|
NM_001190233.1:c.55-1G>C
|
NP_001177162.1:n.55-1G>C
|
|
|
NM_145261.3:c.130-1G>C
|
NP_660304.1:n.130-1G>C
|
|
|
NR_033721.1:n.250-1G>C
|
|
|
|
NR_033722.1:n.301+1000G>C
|
|
|
|
NR_033723.1:n.302-1G>C
|
|
|
|
NR_046073.1:n.176-1027G>C
|
|
|
|
NM_145261.4:c.130-1G>C
MANE Select
|
NP_660304.1:n.130-1G>C
|
|
|
NM_001190233.2:c.55-1G>C
|
NP_001177162.1:n.55-1G>C
|
|
|
NR_033721.2:n.212-1G>C
|
|
|
|
NR_033722.2:n.263+1000G>C
|
|
|
