ENST00000261769.10:c.2434G>C
MANE Select
|
ENSP00000261769.4:p.Asp812His
|
|
ENST00000261769.9:c.2434G>C
|
ENSP00000261769.4:p.Asp812His
|
|
ENST00000422392.6:c.2251G>C
|
ENSP00000414946.2:p.Asp751His
|
|
ENST00000562118.1:n.652G>C
|
|
|
ENST00000562836.5:n.2505G>C
|
|
|
ENST00000566510.5:c.*1100G>C
|
ENSP00000458139.1:n.*1100G>C
|
|
ENST00000566612.5:c.*674G>C
|
ENSP00000454782.1:n.*674G>C
|
|
ENST00000611625.4:c.2497G>C
|
ENSP00000481063.1:p.Asp833His
|
|
ENST00000612417.4:c.1853+3238G>C
|
ENSP00000478360.1:n.1853+3238G>C
|
|
ENST00000621016.4:c.1866-4411G>C
|
ENSP00000480664.1:n.1866-4411G>C
|
|
NM_004360.3:c.2434G>C , LRG_301t1:c.2434G>C
|
NP_004351.1:p.Asp812His
|
|
XM_011523488.1:c.1699G>C
|
XP_011521790.1:p.Asp567His
|
|
XM_011523489.1:c.1699G>C
|
XP_011521791.1:p.Asp567His
|
|
NM_001317184.1:c.2251G>C
|
NP_001304113.1:p.Asp751His
|
|
NM_001317185.1:c.886G>C
|
NP_001304114.1:p.Asp296His
|
|
NM_001317186.1:c.469G>C
|
NP_001304115.1:p.Asp157His
|
|
NM_004360.4:c.2434G>C
|
NP_004351.1:p.Asp812His
|
|
NM_004360.5:c.2434G>C
MANE Select
|
NP_004351.1:p.Asp812His
|
|
NM_001317184.2:c.2251G>C
|
NP_001304113.1:p.Asp751His
|
|
NM_001317185.2:c.886G>C
|
NP_001304114.1:p.Asp296His
|
|
NM_001317186.2:c.469G>C
|
NP_001304115.1:p.Asp157His
|
|