ENST00000330062.8:c.656T=
MANE Select
|
ENSP00000331897.4:p.Met219=
|
|
ENST00000330062.7:c.656T=
|
ENSP00000331897.3:p.Met219=
|
|
ENST00000540499.2:c.500T=
|
ENSP00000446147.2:p.Met167=
|
|
ENST00000559482.5:c.329T=
|
ENSP00000453016.1:p.Met110=
|
|
ENST00000560061.1:c.*281T=
|
ENSP00000453254.1:n.*281T=
|
|
NM_001289910.1:c.500T= , LRG_611t1:c.500T=
|
NP_001276839.1:p.Met167=
|
|
NM_001290114.1:c.266T=
|
NP_001277043.1:p.Met89=
|
|
NM_002168.3:c.656T= , LRG_611t2:c.656T=
|
NP_002159.2:p.Met219=
|
|
NM_001290114.2:c.266T=
|
NP_001277043.1:p.Met89=
|
|
NM_002168.4:c.656T=
MANE Select
|
NP_002159.2:p.Met219=
|
|