ENST00000375731.9:c.824C>T
MANE Select
|
ENSP00000364883.5:p.Ala275Val
|
|
ENST00000303617.5:c.737C>T
|
ENSP00000307334.5:p.Ala246Val
|
|
ENST00000375731.8:c.824C>T
|
ENSP00000364883.4:p.Ala275Val
|
|
ENST00000473695.1:n.96C>T
|
|
|
NM_001306190.1:c.737C>T
|
NP_001293119.1:p.Ala246Val
|
|
NM_001698.2:c.824C>T , LRG_449t1:c.824C>T
|
NP_001689.1:p.Ala275Val
|
|
XM_005252066.2:c.854C>T
|
XP_005252123.1:p.Ala285Val
|
|
XM_005252067.3:c.854C>T
|
XP_005252124.1:p.Ala285Val
|
|
XM_005252069.3:c.854C>T
|
XP_005252126.1:p.Ala285Val
|
|
XM_005252073.2:c.362C>T
|
XP_005252130.1:p.Ala121Val
|
|
XM_006717150.2:c.767C>T
|
XP_006717213.1:p.Ala256Val
|
|
XM_011518801.1:c.500C>T
|
XP_011517103.1:p.Ala167Val
|
|
XM_011518802.1:c.497C>T
|
XP_011517104.1:p.Ala166Val
|
|
NM_001351431.1:c.497C>T
|
NP_001338360.1:p.Ala166Val
|
|
NM_001351432.1:c.497C>T
|
NP_001338361.1:p.Ala166Val
|
|
NM_001351433.1:c.497C>T
|
NP_001338362.1:p.Ala166Val
|
|
XM_005252066.3:c.854C>T
|
XP_005252123.1:p.Ala285Val
|
|
XM_005252067.4:c.854C>T
|
XP_005252124.1:p.Ala285Val
|
|
XM_005252069.4:c.854C>T
|
XP_005252126.1:p.Ala285Val
|
|
XM_006717150.3:c.767C>T
|
XP_006717213.1:p.Ala256Val
|
|
XM_017014849.1:c.824C>T
|
XP_016870338.1:p.Ala275Val
|
|
XR_001746328.2:n.1049C>T
|
|
|
XR_001746329.2:n.1001C>T
|
|
|
NM_001698.3:c.824C>T
MANE Select
|
NP_001689.1:p.Ala275Val
|
|
NM_001306190.2:c.737C>T
|
NP_001293119.1:p.Ala246Val
|
|
NM_001351431.2:c.497C>T
|
NP_001338360.1:p.Ala166Val
|
|
NM_001351432.2:c.497C>T
|
NP_001338361.1:p.Ala166Val
|
|
NM_001351433.2:c.497C>T
|
NP_001338362.1:p.Ala166Val
|
|