ENST00000334785.12:c.1431T>C
MANE Select
|
ENSP00000333938.7:p.Ile477=
|
|
ENST00000330010.12:c.1239T>C
|
ENSP00000327363.8:p.Ile413=
|
|
ENST00000334785.11:c.1431T>C
|
ENSP00000333938.7:p.Ile477=
|
|
ENST00000342754.5:c.1130T>C
|
|
|
ENST00000480732.2:n.1005T>C
|
|
|
NM_001172309.1:c.1239T>C
|
NP_001165780.1:p.Ile413=
|
|
NM_144573.3:c.1431T>C , LRG_442t1:c.1431T>C
|
NP_653174.3:p.Ile477=
|
|
XM_005271322.2:c.1431T>C
|
XP_005271379.1:p.Ile477=
|
|
XM_005271323.2:c.1389T>C
|
XP_005271380.1:p.Ile463=
|
|
XM_005271324.3:c.1239T>C
|
XP_005271381.1:p.Ile413=
|
|
XM_005271325.2:c.1251+2523T>C
|
XP_005271382.1:n.1251+2523T>C
|
|
XM_005271326.2:c.1197T>C
|
XP_005271383.1:p.Ile399=
|
|
XM_005271327.2:c.1014T>C
|
XP_005271384.1:p.Ile338=
|
|
XM_005271322.4:c.1431T>C
|
XP_005271379.1:p.Ile477=
|
|
XM_005271323.4:c.1389T>C
|
XP_005271380.1:p.Ile463=
|
|
XM_005271324.5:c.1239T>C
|
XP_005271381.1:p.Ile413=
|
|
XM_005271325.4:c.1251+2523T>C
|
XP_005271382.1:n.1251+2523T>C
|
|
XM_005271326.4:c.1197T>C
|
XP_005271383.1:p.Ile399=
|
|
XM_005271327.4:c.1014T>C
|
XP_005271384.1:p.Ile338=
|
|
NM_001172309.2:c.1239T>C
|
NP_001165780.1:p.Ile413=
|
|
NM_144573.4:c.1431T>C
MANE Select
|
NP_653174.3:p.Ile477=
|
|