ENST00000435881.7:c.685C>G
MANE Select
|
ENSP00000416627.1:p.Arg229Gly
|
|
ENST00000246912.8:c.847C>G
|
ENSP00000246912.3:p.Arg283Gly
|
|
ENST00000346833.8:c.595C>G
|
ENSP00000320913.3:p.Arg199Gly
|
|
ENST00000435881.6:c.685C>G
|
ENSP00000416627.1:p.Arg229Gly
|
|
ENST00000585403.5:n.892C>G
|
|
|
ENST00000588320.1:n.1161C>G
|
|
|
ENST00000590050.5:n.851C>G
|
|
|
NM_170607.2:c.847C>G
|
NP_733752.1:p.Arg283Gly
|
|
NM_198204.1:c.685C>G
|
NP_937847.1:p.Arg229Gly
|
|
NM_198205.1:c.595C>G
|
NP_937848.1:p.Arg199Gly
|
|
NM_198204.2:c.685C>G
MANE Select
|
NP_937847.1:p.Arg229Gly
|
|
NM_170607.3:c.847C>G
|
NP_733752.1:p.Arg283Gly
|
|
NM_198205.2:c.595C>G
|
NP_937848.1:p.Arg199Gly
|
|