|
NM_000107.3:c.127+5T>G
MANE Select
|
NP_000098.1:n.127+5T>G
|
|
ENST00000256996.9:c.127+5T>G
MANE Select
|
ENSP00000256996.4:n.127+5T>G
|
|
NM_000107.2:c.127+5T>G , LRG_467t1:c.127+5T>G
|
NP_000098.1:n.127+5T>G
|
|
NM_001300734.1:c.127+5T>G
|
NP_001287663.1:n.127+5T>G
|
|
NM_001300734.2:c.127+5T>G
|
NP_001287663.1:n.127+5T>G
|
|
NM_001399874.1:c.127+5T>G
|
NP_001386803.1:n.127+5T>G
|
|
NM_001399875.1:c.127+5T>G
|
NP_001386804.1:n.127+5T>G
|
|
NM_001399876.1:c.127+5T>G
|
NP_001386805.1:n.127+5T>G
|
|
NM_001399878.1:c.127+5T>G
|
NP_001386807.1:n.127+5T>G
|
|
NR_174610.1:n.414+5T>G
|
|
|
NR_174611.1:n.414+5T>G
|
|
|
ENST00000256996.8:c.127+5T>G
|
ENSP00000256996.3:n.127+5T>G
|
|
ENST00000378600.7:c.127+5T>G
|
ENSP00000367863.3:n.127+5T>G
|
|
ENST00000378601.7:c.127+5T>G
|
ENSP00000367864.3:n.127+5T>G
|
|
ENST00000378603.7:c.127+5T>G
|
ENSP00000367866.3:n.127+5T>G
|
|
ENST00000610805.4:c.127+5T>G
|
ENSP00000478063.1:n.127+5T>G
|
|
ENST00000612309.4:n.174T>G
|
|
|
ENST00000614825.4:c.127+5T>G
|
ENSP00000483718.1:n.127+5T>G
|
|
ENST00000615695.1:n.206+5T>G
|
|
|
ENST00000616278.4:c.127+5T>G
|
ENSP00000478411.1:n.127+5T>G
|
|
ENST00000617022.4:n.157T>G
|
|
|
ENST00000622090.4:c.132T>G
|
ENSP00000479994.1:p.Thr44=
|
|
ENST00000622878.4:c.127+5T>G
|
ENSP00000479196.1:n.127+5T>G
|
|
XR_242780.3:n.295+5T>G
|
|
|
XR_242780.4:n.295+5T>G
|
|