ENST00000309383.6:c.2127C>G
MANE Select
|
ENSP00000310649.1:p.Ile709Met
|
|
ENST00000309383.5:c.2127C>G
|
ENSP00000310649.1:p.Ile709Met
|
|
ENST00000326848.7:c.1212C>G
|
ENSP00000320853.7:p.Ile404Met
|
|
ENST00000590333.5:c.2175C>G
|
ENSP00000468190.1:p.Ile725Met
|
|
NM_032430.1:c.2127C>G
|
NP_115806.1:p.Ile709Met
|
|
XM_005259327.2:c.1857C>G
|
XP_005259384.1:p.Ile619Met
|
|
XM_011527395.1:c.1884C>G
|
XP_011525697.1:p.Ile628Met
|
|
XR_430213.2:n.2110C>G
|
|
|
XM_005259327.3:c.1857C>G
|
XP_005259384.1:p.Ile619Met
|
|
XM_011527395.2:c.1599C>G
|
XP_011525697.2:p.Ile533Met
|
|
XM_024451739.1:c.1902C>G
|
XP_024307507.1:p.Ile634Met
|
|
XR_430213.4:n.2408C>G
|
|
|
NM_032430.2:c.2127C>G
MANE Select
|
NP_115806.1:p.Ile709Met
|
|