ENST00000256996.9:c.1010T>G
MANE Select
|
ENSP00000256996.4:p.Leu337Arg
|
|
ENST00000256996.8:c.1010T>G
|
ENSP00000256996.3:p.Leu337Arg
|
|
ENST00000378600.7:c.457-2438T>G
|
ENSP00000367863.3:n.457-2438T>G
|
|
ENST00000378601.7:c.*97T>G
|
ENSP00000367864.3:n.*97T>G
|
|
ENST00000378603.7:c.818T>G
|
ENSP00000367866.3:p.Leu273Arg
|
|
ENST00000612309.4:n.2459T>G
|
|
|
ENST00000614394.1:n.400T>G
|
|
|
ENST00000616278.4:c.686T>G
|
ENSP00000478411.1:n.686T>G
|
|
ENST00000617022.4:n.1554-2438T>G
|
|
|
ENST00000617847.4:c.939T>G
|
|
|
ENST00000620515.1:n.176T>G
|
|
|
NM_000107.2:c.1010T>G , LRG_467t1:c.1010T>G
|
NP_000098.1:p.Leu337Arg
|
|
NM_001300734.1:c.457-2438T>G
|
NP_001287663.1:n.457-2438T>G
|
|
XR_242780.3:n.1000T>G
|
|
|
XR_242780.4:n.1000T>G
|
|
|
NM_000107.3:c.1010T>G
MANE Select
|
NP_000098.1:p.Leu337Arg
|
|
NM_001300734.2:c.457-2438T>G
|
NP_001287663.1:n.457-2438T>G
|
|
NM_001399874.1:c.1010T>G
|
NP_001386803.1:p.Leu337Arg
|
|
NM_001399875.1:c.1010T>G
|
NP_001386804.1:p.Leu337Arg
|
|
NM_001399876.1:c.457-2438T>G
|
NP_001386805.1:n.457-2438T>G
|
|
NM_001399878.1:c.818T>G
|
NP_001386807.1:p.Leu273Arg
|
|
NR_174610.1:n.1261T>G
|
|
|
NR_174611.1:n.1239T>G
|
|
|