ENST00000256996.9:c.963C>T
MANE Select
|
ENSP00000256996.4:p.Asp321=
|
|
ENST00000256996.8:c.963C>T
|
ENSP00000256996.3:p.Asp321=
|
|
ENST00000378600.7:c.457-2485C>T
|
ENSP00000367863.3:n.457-2485C>T
|
|
ENST00000378601.7:c.*50C>T
|
ENSP00000367864.3:n.*50C>T
|
|
ENST00000378603.7:c.771C>T
|
ENSP00000367866.3:p.Asp257=
|
|
ENST00000612309.4:n.2412C>T
|
|
|
ENST00000614394.1:n.353C>T
|
|
|
ENST00000616278.4:c.639C>T
|
ENSP00000478411.1:n.639C>T
|
|
ENST00000617022.4:n.1554-2485C>T
|
|
|
ENST00000617847.4:c.892C>T
|
|
|
ENST00000620515.1:n.129C>T
|
|
|
NM_000107.2:c.963C>T , LRG_467t1:c.963C>T
|
NP_000098.1:p.Asp321=
|
|
NM_001300734.1:c.457-2485C>T
|
NP_001287663.1:n.457-2485C>T
|
|
XR_242780.3:n.953C>T
|
|
|
XR_242780.4:n.953C>T
|
|
|
NM_000107.3:c.963C>T
MANE Select
|
NP_000098.1:p.Asp321=
|
|
NM_001300734.2:c.457-2485C>T
|
NP_001287663.1:n.457-2485C>T
|
|
NM_001399874.1:c.963C>T
|
NP_001386803.1:p.Asp321=
|
|
NM_001399875.1:c.963C>T
|
NP_001386804.1:p.Asp321=
|
|
NM_001399876.1:c.457-2485C>T
|
NP_001386805.1:n.457-2485C>T
|
|
NM_001399878.1:c.771C>T
|
NP_001386807.1:p.Asp257=
|
|
NR_174610.1:n.1214C>T
|
|
|
NR_174611.1:n.1192C>T
|
|
|