ENST00000262407.6:c.3060+86C>T
MANE Select
|
ENSP00000262407.5:n.3060+86C>T
|
|
ENST00000648408.1:c.2374+391C>T
|
|
|
ENST00000262407.5:c.3060+86C>T
|
ENSP00000262407.5:n.3060+86C>T
|
|
ENST00000587295.5:c.253+1565C>T
|
|
|
ENST00000588098.1:c.37+391C>T
|
|
|
ENST00000592462.5:n.2845C>T
|
|
|
NM_000419.3:c.3060+86C>T , LRG_479t1:c.3060+86C>T
|
NP_000410.2:n.3060+86C>T
|
|
XM_011524749.1:c.2958+86C>T
|
XP_011523051.1:n.2958+86C>T
|
|
XM_011524750.1:c.2943+391C>T
|
XP_011523052.1:n.2943+391C>T
|
|
NM_000419.4:c.3060+86C>T
|
NP_000410.2:n.3060+86C>T
|
|
NM_000419.5:c.3060+86C>T
MANE Select
|
NP_000410.2:n.3060+86C>T
|
|