|
NM_000107.3:c.1187C>A
MANE Select
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NP_000098.1:p.Ser396Ter
|
|
ENST00000256996.9:c.1187C>A
MANE Select
|
ENSP00000256996.4:p.Ser396Ter
|
|
NM_000107.2:c.1187C>A , LRG_467t1:c.1187C>A
|
NP_000098.1:p.Ser396Ter
|
|
NM_001300734.1:c.620C>A
|
NP_001287663.1:p.Ser207Ter
|
|
NM_001300734.2:c.620C>A
|
NP_001287663.1:p.Ser207Ter
|
|
NM_001399874.1:c.1187C>A
|
NP_001386803.1:p.Ser396Ter
|
|
NM_001399875.1:c.1187C>A
|
NP_001386804.1:p.Ser396Ter
|
|
NM_001399876.1:c.620C>A
|
NP_001386805.1:p.Ser207Ter
|
|
NM_001399878.1:c.995C>A
|
NP_001386807.1:p.Ser332Ter
|
|
NR_174610.1:n.1438C>A
|
|
|
NR_174611.1:n.1416C>A
|
|
|
ENST00000256996.8:c.1187C>A
|
ENSP00000256996.3:p.Ser396Ter
|
|
ENST00000378600.7:c.620C>A
|
ENSP00000367863.3:p.Ser207Ter
|
|
ENST00000378601.7:c.*274C>A
|
ENSP00000367864.3:n.*274C>A
|
|
ENST00000378603.7:c.995C>A
|
ENSP00000367866.3:p.Ser332Ter
|
|
ENST00000612309.4:n.2636C>A
|
|
|
ENST00000614884.1:n.195C>A
|
|
|
ENST00000616278.4:c.863C>A
|
ENSP00000478411.1:n.863C>A
|
|
ENST00000617022.4:n.1717C>A
|
|
|
ENST00000617847.4:c.1210C>A
|
|
|
XR_242780.3:n.1177C>A
|
|
|
XR_242780.4:n.1177C>A
|
|