ENST00000370274.8:c.935T>G
MANE Select
|
ENSP00000359297.3:p.Met312Arg
|
|
ENST00000370274.7:c.935T>G
|
ENSP00000359297.3:p.Met312Arg
|
|
ENST00000440023.5:c.935T>G
|
ENSP00000391854.1:p.Met312Arg
|
|
NM_001129765.1:c.935T>G
|
NP_001123237.1:p.Met312Arg
|
|
NM_015922.2:c.935T>G
|
NP_057006.1:p.Met312Arg
|
|
XM_011531178.1:c.935T>G
|
XP_011529480.1:p.Met312Arg
|
|
XM_011531178.2:c.935T>G
|
XP_011529480.1:p.Met312Arg
|
|
XM_017029564.1:c.983T>G
|
XP_016885053.1:p.Met328Arg
|
|
NM_015922.3:c.935T>G
MANE Select
|
NP_057006.1:p.Met312Arg
|
|
NM_001129765.2:c.935T>G
|
NP_001123237.1:p.Met312Arg
|
|