ENST00000375448.4:c.1369C>G
MANE Select
|
ENSP00000364597.4:p.Gln457Glu
|
|
ENST00000467001.1:n.270C>G
|
|
|
ENST00000487048.5:n.336C>G
|
|
|
NM_012387.2:c.1369C>G
|
NP_036519.2:p.Gln457Glu
|
|
XM_011541150.1:c.1183C>G
|
XP_011539452.1:p.Gln395Glu
|
|
XM_011541151.1:c.1156-316C>G
|
XP_011539453.1:n.1156-316C>G
|
|
XM_011541152.1:c.832C>G
|
XP_011539454.1:p.Gln278Glu
|
|
XM_011541154.1:c.*106C>G
|
XP_011539456.1:n.*106C>G
|
|
XM_011541156.1:c.*53C>G
|
XP_011539458.1:n.*53C>G
|
|
XM_011541157.1:c.478C>G
|
XP_011539459.1:p.Gln160Glu
|
|
XM_011541154.2:c.*106C>G
|
XP_011539456.1:n.*106C>G
|
|
NM_012387.3:c.1369C>G
MANE Select
|
NP_036519.2:p.Gln457Glu
|
|