ENST00000638375.2:c.1376A>C
|
ENSP00000492789.2:n.1376A>C
|
|
ENST00000706899.1:n.2347A>C
|
|
|
ENST00000706900.1:c.*395A>C
|
ENSP00000516617.1:n.*395A>C
|
|
ENST00000706901.1:c.*395A>C
|
ENSP00000516612.1:n.*395A>C
|
|
ENST00000706902.1:c.1093+569A>C
|
ENSP00000516613.1:n.1093+569A>C
|
|
ENST00000706903.1:c.*124+271A>C
|
ENSP00000516614.1:n.*124+271A>C
|
|
ENST00000706904.1:c.1093+569A>C
|
ENSP00000516615.1:n.1093+569A>C
|
|
ENST00000706905.1:c.*395A>C
|
ENSP00000516616.1:n.*395A>C
|
|
ENST00000376809.10:c.*395A>C
MANE Select
|
ENSP00000366005.5:n.*395A>C
|
|
ENST00000376802.2:c.*395A>C
|
ENSP00000365998.2:n.*395A>C
|
|
ENST00000376806.9:c.*395A>C
|
ENSP00000366002.5:n.*395A>C
|
|
ENST00000376809.9:c.*395A>C
|
ENSP00000366005.5:n.*395A>C
|
|
ENST00000396634.5:c.*395A>C
|
ENSP00000379873.1:n.*395A>C
|
|
ENST00000495183.5:n.1732A>C
|
|
|
ENST00000496081.5:n.1752A>C
|
|
|
NM_002116.7:c.*395A>C
|
NP_002107.3:n.*395A>C
|
|
NM_002116.8:c.*395A>C
MANE Select
|
NP_002107.3:n.*395A>C
|
|