|
ENST00000261769.10:c.2644G>C
MANE Select
|
ENSP00000261769.4:p.Asp882His
|
|
|
ENST00000261769.9:c.2644G>C
|
ENSP00000261769.4:p.Asp882His
|
|
|
ENST00000422392.6:c.2461G>C
|
ENSP00000414946.2:p.Asp821His
|
|
|
ENST00000562118.1:n.862G>C
|
|
|
|
ENST00000562836.5:n.2715G>C
|
|
|
|
ENST00000566510.5:c.*1310G>C
|
ENSP00000458139.1:n.*1310G>C
|
|
|
ENST00000566612.5:c.*884G>C
|
ENSP00000454782.1:n.*884G>C
|
|
|
ENST00000611625.4:c.2707G>C
|
ENSP00000481063.1:p.Asp903His
|
|
|
ENST00000612417.4:c.1854-697G>C
|
ENSP00000478360.1:n.1854-697G>C
|
|
|
ENST00000621016.4:c.1866-709G>C
|
ENSP00000480664.1:n.1866-709G>C
|
|
|
NM_004360.3:c.2644G>C , LRG_301t1:c.2644G>C
|
NP_004351.1:p.Asp882His
|
|
|
XM_011523488.1:c.1909G>C
|
XP_011521790.1:p.Asp637His
|
|
|
XM_011523489.1:c.1909G>C
|
XP_011521791.1:p.Asp637His
|
|
|
NM_001317184.1:c.2461G>C
|
NP_001304113.1:p.Asp821His
|
|
|
NM_001317185.1:c.1096G>C
|
NP_001304114.1:p.Asp366His
|
|
|
NM_001317186.1:c.679G>C
|
NP_001304115.1:p.Asp227His
|
|
|
NM_004360.4:c.2644G>C
|
NP_004351.1:p.Asp882His
|
|
|
NM_004360.5:c.2644G>C
MANE Select
|
NP_004351.1:p.Asp882His
|
|
|
NM_001317184.2:c.2461G>C
|
NP_001304113.1:p.Asp821His
|
|
|
NM_001317185.2:c.1096G>C
|
NP_001304114.1:p.Asp366His
|
|
|
NM_001317186.2:c.679G>C
|
NP_001304115.1:p.Asp227His
|
|
