ENST00000375731.9:c.823G>A
MANE Select
|
ENSP00000364883.5:p.Ala275Thr
|
|
ENST00000303617.5:c.736G>A
|
ENSP00000307334.5:p.Ala246Thr
|
|
ENST00000375731.8:c.823G>A
|
ENSP00000364883.4:p.Ala275Thr
|
|
ENST00000473695.1:n.95G>A
|
|
|
NM_001306190.1:c.736G>A
|
NP_001293119.1:p.Ala246Thr
|
|
NM_001698.2:c.823G>A , LRG_449t1:c.823G>A
|
NP_001689.1:p.Ala275Thr
|
|
XM_005252066.2:c.853G>A
|
XP_005252123.1:p.Ala285Thr
|
|
XM_005252067.3:c.853G>A
|
XP_005252124.1:p.Ala285Thr
|
|
XM_005252069.3:c.853G>A
|
XP_005252126.1:p.Ala285Thr
|
|
XM_005252073.2:c.361G>A
|
XP_005252130.1:p.Ala121Thr
|
|
XM_006717150.2:c.766G>A
|
XP_006717213.1:p.Ala256Thr
|
|
XM_011518801.1:c.499G>A
|
XP_011517103.1:p.Ala167Thr
|
|
XM_011518802.1:c.496G>A
|
XP_011517104.1:p.Ala166Thr
|
|
NM_001351431.1:c.496G>A
|
NP_001338360.1:p.Ala166Thr
|
|
NM_001351432.1:c.496G>A
|
NP_001338361.1:p.Ala166Thr
|
|
NM_001351433.1:c.496G>A
|
NP_001338362.1:p.Ala166Thr
|
|
XM_005252066.3:c.853G>A
|
XP_005252123.1:p.Ala285Thr
|
|
XM_005252067.4:c.853G>A
|
XP_005252124.1:p.Ala285Thr
|
|
XM_005252069.4:c.853G>A
|
XP_005252126.1:p.Ala285Thr
|
|
XM_006717150.3:c.766G>A
|
XP_006717213.1:p.Ala256Thr
|
|
XM_017014849.1:c.823G>A
|
XP_016870338.1:p.Ala275Thr
|
|
XR_001746328.2:n.1048G>A
|
|
|
XR_001746329.2:n.1000G>A
|
|
|
NM_001698.3:c.823G>A
MANE Select
|
NP_001689.1:p.Ala275Thr
|
|
NM_001306190.2:c.736G>A
|
NP_001293119.1:p.Ala246Thr
|
|
NM_001351431.2:c.496G>A
|
NP_001338360.1:p.Ala166Thr
|
|
NM_001351432.2:c.496G>A
|
NP_001338361.1:p.Ala166Thr
|
|
NM_001351433.2:c.496G>A
|
NP_001338362.1:p.Ala166Thr
|
|