ENST00000309383.6:c.2126T>G
MANE Select
|
ENSP00000310649.1:p.Ile709Ser
|
|
ENST00000309383.5:c.2126T>G
|
ENSP00000310649.1:p.Ile709Ser
|
|
ENST00000326848.7:c.1211T>G
|
ENSP00000320853.7:p.Ile404Ser
|
|
ENST00000590333.5:c.2174T>G
|
ENSP00000468190.1:p.Ile725Ser
|
|
NM_032430.1:c.2126T>G
|
NP_115806.1:p.Ile709Ser
|
|
XM_005259327.2:c.1856T>G
|
XP_005259384.1:p.Ile619Ser
|
|
XM_011527395.1:c.1883T>G
|
XP_011525697.1:p.Ile628Ser
|
|
XR_430213.2:n.2109T>G
|
|
|
XM_005259327.3:c.1856T>G
|
XP_005259384.1:p.Ile619Ser
|
|
XM_011527395.2:c.1598T>G
|
XP_011525697.2:p.Ile533Ser
|
|
XM_024451739.1:c.1901T>G
|
XP_024307507.1:p.Ile634Ser
|
|
XR_430213.4:n.2407T>G
|
|
|
NM_032430.2:c.2126T>G
MANE Select
|
NP_115806.1:p.Ile709Ser
|
|