|
NM_002168.4:c.1189A>G
MANE Select
|
NP_002159.2:p.Met397Val
|
|
ENST00000330062.8:c.1189A>G
MANE Select
|
ENSP00000331897.4:p.Met397Val
|
|
NM_001289910.1:c.1033A>G , LRG_611t1:c.1033A>G
|
NP_001276839.1:p.Met345Val
|
|
NM_001290114.1:c.799A>G
|
NP_001277043.1:p.Met267Val
|
|
NM_001290114.2:c.799A>G
|
NP_001277043.1:p.Met267Val
|
|
NM_002168.3:c.1189A>G , LRG_611t2:c.1189A>G
|
NP_002159.2:p.Met397Val
|
|
ENST00000330062.7:c.1189A>G
|
ENSP00000331897.3:p.Met397Val
|
|
ENST00000540499.2:c.1033A>G
|
ENSP00000446147.2:p.Met345Val
|
|
ENST00000559482.5:c.851+103A>G
|
ENSP00000453016.1:n.851+103A>G
|
|
ENST00000560061.1:c.*814A>G
|
ENSP00000453254.1:n.*814A>G
|