ENST00000622290.5:c.*574C>G
|
ENSP00000483331.2:n.*574C>G
|
|
ENST00000205557.12:c.4402C>G
MANE Select
|
ENSP00000205557.7:p.Arg1468Gly
|
|
ENST00000640696.1:c.1216C>G
|
ENSP00000492197.1:p.Arg406Gly
|
|
ENST00000205557.11:c.4402C>G
|
ENSP00000205557.7:p.Arg1468Gly
|
|
ENST00000456970.6:c.4027C>G
|
ENSP00000405002.2:n.4027C>G
|
|
ENST00000576204.5:n.1265C>G
|
|
|
ENST00000622290.4:c.*1611C>G
|
ENSP00000483331.1:n.*1611C>G
|
|
NM_001171.5:c.4402C>G
|
NP_001162.4:p.Arg1468Gly
|
|
XM_011522479.1:c.4369C>G
|
XP_011520781.1:p.Arg1457Gly
|
|
XM_011522480.1:c.4060C>G
|
XP_011520782.1:p.Arg1354Gly
|
|
XM_011522481.1:c.4060C>G
|
XP_011520783.1:p.Arg1354Gly
|
|
XR_933134.1:n.538+6289G>C
|
|
|
NM_001351800.1:c.4060C>G
|
NP_001338729.1:p.Arg1354Gly
|
|
NR_147784.1:n.4064C>G
|
|
|
XM_011522479.2:c.4369C>G
|
XP_011520781.1:p.Arg1457Gly
|
|
XM_011522481.3:c.4060C>G
|
XP_011520783.1:p.Arg1354Gly
|
|
XM_017023212.1:c.4234C>G
|
XP_016878701.1:p.Arg1412Gly
|
|
XM_024450261.1:c.4438C>G
|
XP_024306029.1:p.Arg1480Gly
|
|
NM_001171.6:c.4402C>G
MANE Select
|
NP_001162.5:p.Arg1468Gly
|
|