ENST00000259216.6:c.664C>G
MANE Select
|
ENSP00000259216.5:p.Arg222Gly
|
|
ENST00000259216.4:c.664C>G
|
ENSP00000259216.4:p.Arg222Gly
|
|
ENST00000615342.4:c.549C>G
|
ENSP00000480526.1:p.Ile183Met
|
|
ENST00000621673.4:c.439C>G
|
ENSP00000480843.1:p.Arg147Gly
|
|
NM_001270420.1:c.549C>G
|
NP_001257349.1:p.Ile183Met
|
|
NM_001270421.1:c.439C>G
|
NP_001257350.1:p.Arg147Gly
|
|
NM_032545.3:c.664C>G
|
NP_115934.1:p.Arg222Gly
|
|
NM_032545.4:c.664C>G
MANE Select
|
NP_115934.1:p.Arg222Gly
|
|
NM_001270420.2:c.549C>G
|
NP_001257349.1:p.Ile183Met
|
|
NM_001270421.2:c.439C>G
|
NP_001257350.1:p.Arg147Gly
|
|