ENST00000330062.8:c.656T>G
MANE Select
|
ENSP00000331897.4:p.Met219Arg
|
|
ENST00000330062.7:c.656T>G
|
ENSP00000331897.3:p.Met219Arg
|
|
ENST00000540499.2:c.500T>G
|
ENSP00000446147.2:p.Met167Arg
|
|
ENST00000559482.5:c.329T>G
|
ENSP00000453016.1:p.Met110Arg
|
|
ENST00000560061.1:c.*281T>G
|
ENSP00000453254.1:n.*281T>G
|
|
NM_001289910.1:c.500T>G , LRG_611t1:c.500T>G
|
NP_001276839.1:p.Met167Arg
|
|
NM_001290114.1:c.266T>G
|
NP_001277043.1:p.Met89Arg
|
|
NM_002168.3:c.656T>G , LRG_611t2:c.656T>G
|
NP_002159.2:p.Met219Arg
|
|
NM_001290114.2:c.266T>G
|
NP_001277043.1:p.Met89Arg
|
|
NM_002168.4:c.656T>G
MANE Select
|
NP_002159.2:p.Met219Arg
|
|