|
NM_001698.3:c.556G>T
MANE Select
|
NP_001689.1:p.Gly186Cys
|
|
ENST00000375731.9:c.556G>T
MANE Select
|
ENSP00000364883.5:p.Gly186Cys
|
|
NM_001306190.1:c.469G>T
|
NP_001293119.1:p.Gly157Cys
|
|
NM_001306190.2:c.469G>T
|
NP_001293119.1:p.Gly157Cys
|
|
NM_001351431.1:c.229G>T
|
NP_001338360.1:p.Gly77Cys
|
|
NM_001351431.2:c.229G>T
|
NP_001338360.1:p.Gly77Cys
|
|
NM_001351432.1:c.229G>T
|
NP_001338361.1:p.Gly77Cys
|
|
NM_001351432.2:c.229G>T
|
NP_001338361.1:p.Gly77Cys
|
|
NM_001351433.1:c.229G>T
|
NP_001338362.1:p.Gly77Cys
|
|
NM_001351433.2:c.229G>T
|
NP_001338362.1:p.Gly77Cys
|
|
NM_001698.2:c.556G>T , LRG_449t1:c.556G>T
|
NP_001689.1:p.Gly186Cys
|
|
ENST00000303617.5:c.469G>T
|
ENSP00000307334.5:p.Gly157Cys
|
|
ENST00000375731.8:c.556G>T
|
ENSP00000364883.4:p.Gly186Cys
|
|
ENST00000478465.5:n.716G>T
|
|
|
XM_005252066.2:c.586G>T
|
XP_005252123.1:p.Gly196Cys
|
|
XM_005252066.3:c.586G>T
|
XP_005252123.1:p.Gly196Cys
|
|
XM_005252067.3:c.586G>T
|
XP_005252124.1:p.Gly196Cys
|
|
XM_005252067.4:c.586G>T
|
XP_005252124.1:p.Gly196Cys
|
|
XM_005252069.3:c.586G>T
|
XP_005252126.1:p.Gly196Cys
|
|
XM_005252069.4:c.586G>T
|
XP_005252126.1:p.Gly196Cys
|
|
XM_005252072.1:c.556G>T
|
XP_005252129.1:p.Gly186Cys
|
|
XM_005252072.2:c.556G>T
|
XP_005252129.1:p.Gly186Cys
|
|
XM_005252073.2:c.94G>T
|
XP_005252130.1:p.Gly32Cys
|
|
XM_006717150.2:c.499G>T
|
XP_006717213.1:p.Gly167Cys
|
|
XM_006717150.3:c.499G>T
|
XP_006717213.1:p.Gly167Cys
|
|
XM_011518800.1:c.586G>T
|
XP_011517102.1:p.Gly196Cys
|
|
XM_011518800.3:c.586G>T
|
XP_011517102.1:p.Gly196Cys
|
|
XM_011518801.1:c.232G>T
|
XP_011517103.1:p.Gly78Cys
|
|
XM_011518802.1:c.229G>T
|
XP_011517104.1:p.Gly77Cys
|
|
XM_017014849.1:c.556G>T
|
XP_016870338.1:p.Gly186Cys
|
|
XR_001746328.2:n.639G>T
|
|
|
XR_001746329.2:n.591G>T
|
|
