ENST00000262507.11:c.34C>G
MANE Select
|
ENSP00000262507.5:p.Arg12Gly
|
|
ENST00000262507.10:c.34C>G
|
ENSP00000262507.5:p.Arg12Gly
|
|
ENST00000562426.5:n.37C>G
|
|
|
ENST00000562734.5:n.58C>G
|
|
|
ENST00000564115.5:c.34C>G
|
ENSP00000455256.1:p.Arg12Gly
|
|
ENST00000564655.5:c.34C>G
|
ENSP00000454992.1:p.Arg12Gly
|
|
ENST00000565964.5:c.34C>G
|
ENSP00000458023.1:p.Arg12Gly
|
|
ENST00000566388.5:n.115C>G
|
|
|
ENST00000567072.5:c.34C>G
|
ENSP00000456728.1:p.Arg12Gly
|
|
ENST00000567933.5:c.34C>G
|
ENSP00000456174.1:p.Arg12Gly
|
|
ENST00000568790.5:n.58C>G
|
|
|
NM_020312.3:c.34C>G
|
NP_064708.1:p.Arg12Gly
|
|
NM_020312.4:c.34C>G
MANE Select
|
NP_064708.1:p.Arg12Gly
|
|