ENST00000334785.12:c.1442T>G
MANE Select
|
ENSP00000333938.7:p.Ile481Ser
|
|
ENST00000330010.12:c.1250T>G
|
ENSP00000327363.8:p.Ile417Ser
|
|
ENST00000334785.11:c.1442T>G
|
ENSP00000333938.7:p.Ile481Ser
|
|
ENST00000342754.5:c.1141T>G
|
|
|
ENST00000480732.2:n.1016T>G
|
|
|
NM_001172309.1:c.1250T>G
|
NP_001165780.1:p.Ile417Ser
|
|
NM_144573.3:c.1442T>G , LRG_442t1:c.1442T>G
|
NP_653174.3:p.Ile481Ser
|
|
XM_005271322.2:c.1442T>G
|
XP_005271379.1:p.Ile481Ser
|
|
XM_005271323.2:c.1400T>G
|
XP_005271380.1:p.Ile467Ser
|
|
XM_005271324.3:c.1250T>G
|
XP_005271381.1:p.Ile417Ser
|
|
XM_005271325.2:c.1251+2534T>G
|
XP_005271382.1:n.1251+2534T>G
|
|
XM_005271326.2:c.1208T>G
|
XP_005271383.1:p.Ile403Ser
|
|
XM_005271327.2:c.1025T>G
|
XP_005271384.1:p.Ile342Ser
|
|
XM_005271322.4:c.1442T>G
|
XP_005271379.1:p.Ile481Ser
|
|
XM_005271323.4:c.1400T>G
|
XP_005271380.1:p.Ile467Ser
|
|
XM_005271324.5:c.1250T>G
|
XP_005271381.1:p.Ile417Ser
|
|
XM_005271325.4:c.1251+2534T>G
|
XP_005271382.1:n.1251+2534T>G
|
|
XM_005271326.4:c.1208T>G
|
XP_005271383.1:p.Ile403Ser
|
|
XM_005271327.4:c.1025T>G
|
XP_005271384.1:p.Ile342Ser
|
|
NM_001172309.2:c.1250T>G
|
NP_001165780.1:p.Ile417Ser
|
|
NM_144573.4:c.1442T>G
MANE Select
|
NP_653174.3:p.Ile481Ser
|
|