ENST00000256996.9:c.961G>C
MANE Select
|
ENSP00000256996.4:p.Asp321His
|
|
ENST00000256996.8:c.961G>C
|
ENSP00000256996.3:p.Asp321His
|
|
ENST00000378600.7:c.457-2487G>C
|
ENSP00000367863.3:n.457-2487G>C
|
|
ENST00000378601.7:c.*48G>C
|
ENSP00000367864.3:n.*48G>C
|
|
ENST00000378603.7:c.769G>C
|
ENSP00000367866.3:p.Asp257His
|
|
ENST00000612309.4:n.2410G>C
|
|
|
ENST00000614394.1:n.351G>C
|
|
|
ENST00000616278.4:c.637G>C
|
ENSP00000478411.1:n.637G>C
|
|
ENST00000617022.4:n.1554-2487G>C
|
|
|
ENST00000617847.4:c.890G>C
|
|
|
ENST00000620515.1:n.127G>C
|
|
|
NM_000107.2:c.961G>C , LRG_467t1:c.961G>C
|
NP_000098.1:p.Asp321His
|
|
NM_001300734.1:c.457-2487G>C
|
NP_001287663.1:n.457-2487G>C
|
|
XR_242780.3:n.951G>C
|
|
|
XR_242780.4:n.951G>C
|
|
|
NM_000107.3:c.961G>C
MANE Select
|
NP_000098.1:p.Asp321His
|
|
NM_001300734.2:c.457-2487G>C
|
NP_001287663.1:n.457-2487G>C
|
|
NM_001399874.1:c.961G>C
|
NP_001386803.1:p.Asp321His
|
|
NM_001399875.1:c.961G>C
|
NP_001386804.1:p.Asp321His
|
|
NM_001399876.1:c.457-2487G>C
|
NP_001386805.1:n.457-2487G>C
|
|
NM_001399878.1:c.769G>C
|
NP_001386807.1:p.Asp257His
|
|
NR_174610.1:n.1212G>C
|
|
|
NR_174611.1:n.1190G>C
|
|
|