ENST00000615310.5:c.2201C>A
|
ENSP00000480088.2:p.Ala734Asp
|
|
ENST00000683007.1:n.2171C>A
|
|
|
ENST00000683872.1:n.2162C>A
|
|
|
ENST00000340058.6:c.2597C>A
|
ENSP00000344798.4:p.Ala866Asp
|
|
ENST00000355710.8:c.2597C>A
MANE Select
|
ENSP00000347942.3:p.Ala866Asp
|
|
ENST00000671844.1:c.*1191C>A
|
ENSP00000500541.1:n.*1191C>A
|
|
ENST00000672389.1:c.*1191C>A
|
ENSP00000500252.1:n.*1191C>A
|
|
ENST00000340058.5:c.2597C>A
|
ENSP00000344798.4:p.Ala866Asp
|
|
ENST00000355710.7:c.2597C>A
|
ENSP00000347942.3:p.Ala866Asp
|
|
ENST00000615310.4:c.1323C>A
|
ENSP00000480088.1:p.Gly441=
|
|
NM_020630.4:c.2597C>A , LRG_518t2:c.2597C>A
|
NP_065681.1:p.Ala866Asp
|
|
NM_020975.4:c.2597C>A , LRG_518t1:c.2597C>A
|
NP_066124.1:p.Ala866Asp
|
|
XM_011540027.1:c.2597C>A
|
XP_011538329.1:p.Ala866Asp
|
|
NM_001355216.1:c.1835C>A
|
NP_001342145.1:p.Ala612Asp
|
|
NM_020630.5:c.2597C>A
|
NP_065681.1:p.Ala866Asp
|
|
NM_020975.5:c.2597C>A
|
NP_066124.1:p.Ala866Asp
|
|
NM_020975.6:c.2597C>A
MANE Select
|
NP_066124.1:p.Ala866Asp
|
|
NM_020630.6:c.2597C>A
|
NP_065681.1:p.Ala866Asp
|
|