ENST00000503581.6:c.7053C>G
MANE Select
|
ENSP00000424243.1:p.Ile2351Met
|
|
ENST00000370616.6:c.7053C>G
|
ENSP00000359650.2:p.Ile2351Met
|
|
ENST00000370618.7:c.7053C>G
|
ENSP00000359652.4:p.Ile2351Met
|
|
ENST00000370621.7:c.7053C>G
|
ENSP00000359655.3:p.Ile2351Met
|
|
ENST00000398580.3:c.367C>G
|
|
|
ENST00000503581.5:c.7053C>G
|
ENSP00000424243.1:p.Ile2351Met
|
|
NM_001142800.1:c.7053C>G
|
NP_001136272.1:p.Ile2351Met
|
|
NM_001292009.1:c.7053C>G
|
NP_001278938.1:p.Ile2351Met
|
|
XR_001744188.1:n.606+16101G>C
|
|
|
XR_001744189.1:n.129+16101G>C
|
|
|
XR_001744190.1:n.197+16101G>C
|
|
|
XR_001744191.1:n.607-1269G>C
|
|
|
NM_001142800.2:c.7053C>G
MANE Select
|
NP_001136272.1:p.Ile2351Met
|
|
NM_001292009.2:c.7053C>G
|
NP_001278938.1:p.Ile2351Met
|
|