ENST00000330062.8:c.643G>C
MANE Select
|
ENSP00000331897.4:p.Gly215Arg
|
|
ENST00000330062.7:c.643G>C
|
ENSP00000331897.3:p.Gly215Arg
|
|
ENST00000540499.2:c.487G>C
|
ENSP00000446147.2:p.Gly163Arg
|
|
ENST00000559482.5:c.316G>C
|
ENSP00000453016.1:p.Gly106Arg
|
|
ENST00000560061.1:c.*268G>C
|
ENSP00000453254.1:n.*268G>C
|
|
NM_001289910.1:c.487G>C , LRG_611t1:c.487G>C
|
NP_001276839.1:p.Gly163Arg
|
|
NM_001290114.1:c.253G>C
|
NP_001277043.1:p.Gly85Arg
|
|
NM_002168.3:c.643G>C , LRG_611t2:c.643G>C
|
NP_002159.2:p.Gly215Arg
|
|
NM_001290114.2:c.253G>C
|
NP_001277043.1:p.Gly85Arg
|
|
NM_002168.4:c.643G>C
MANE Select
|
NP_002159.2:p.Gly215Arg
|
|