ENST00000261769.10:c.2059G>C
MANE Select
|
ENSP00000261769.4:p.Asp687His
|
|
ENST00000261769.9:c.2059G>C
|
ENSP00000261769.4:p.Asp687His
|
|
ENST00000422392.6:c.1876G>C
|
ENSP00000414946.2:p.Asp626His
|
|
ENST00000562118.1:n.277G>C
|
|
|
ENST00000562836.5:n.2130G>C
|
|
|
ENST00000566510.5:c.*725G>C
|
ENSP00000458139.1:n.*725G>C
|
|
ENST00000566612.5:c.*299G>C
|
ENSP00000454782.1:n.*299G>C
|
|
ENST00000611625.4:c.2122G>C
|
ENSP00000481063.1:p.Asp708His
|
|
ENST00000612417.4:c.1830+1402G>C
|
ENSP00000478360.1:n.1830+1402G>C
|
|
ENST00000621016.4:c.1865+1367G>C
|
ENSP00000480664.1:n.1865+1367G>C
|
|
NM_004360.3:c.2059G>C , LRG_301t1:c.2059G>C
|
NP_004351.1:p.Asp687His
|
|
XM_011523488.1:c.1324G>C
|
XP_011521790.1:p.Asp442His
|
|
XM_011523489.1:c.1324G>C
|
XP_011521791.1:p.Asp442His
|
|
NM_001317184.1:c.1876G>C
|
NP_001304113.1:p.Asp626His
|
|
NM_001317185.1:c.511G>C
|
NP_001304114.1:p.Asp171His
|
|
NM_001317186.1:c.94G>C
|
NP_001304115.1:p.Asp32His
|
|
NM_004360.4:c.2059G>C
|
NP_004351.1:p.Asp687His
|
|
NM_004360.5:c.2059G>C
MANE Select
|
NP_004351.1:p.Asp687His
|
|
NM_001317184.2:c.1876G>C
|
NP_001304113.1:p.Asp626His
|
|
NM_001317185.2:c.511G>C
|
NP_001304114.1:p.Asp171His
|
|
NM_001317186.2:c.94G>C
|
NP_001304115.1:p.Asp32His
|
|