ENST00000615310.5:c.2216T>G
|
ENSP00000480088.2:p.Val739Gly
|
|
ENST00000683007.1:n.2186T>G
|
|
|
ENST00000683872.1:n.2177T>G
|
|
|
ENST00000340058.6:c.2612T>G
|
ENSP00000344798.4:p.Val871Gly
|
|
ENST00000355710.8:c.2612T>G
MANE Select
|
ENSP00000347942.3:p.Val871Gly
|
|
ENST00000671844.1:c.*1206T>G
|
ENSP00000500541.1:n.*1206T>G
|
|
ENST00000672389.1:c.*1206T>G
|
ENSP00000500252.1:n.*1206T>G
|
|
ENST00000340058.5:c.2612T>G
|
ENSP00000344798.4:p.Val871Gly
|
|
ENST00000355710.7:c.2612T>G
|
ENSP00000347942.3:p.Val871Gly
|
|
ENST00000615310.4:c.1338T>G
|
ENSP00000480088.1:p.Arg446=
|
|
NM_020630.4:c.2612T>G , LRG_518t2:c.2612T>G
|
NP_065681.1:p.Val871Gly
|
|
NM_020975.4:c.2612T>G , LRG_518t1:c.2612T>G
|
NP_066124.1:p.Val871Gly
|
|
XM_011540027.1:c.2612T>G
|
XP_011538329.1:p.Val871Gly
|
|
NM_001355216.1:c.1850T>G
|
NP_001342145.1:p.Val617Gly
|
|
NM_020630.5:c.2612T>G
|
NP_065681.1:p.Val871Gly
|
|
NM_020975.5:c.2612T>G
|
NP_066124.1:p.Val871Gly
|
|
NM_020975.6:c.2612T>G
MANE Select
|
NP_066124.1:p.Val871Gly
|
|
NM_020630.6:c.2612T>G
|
NP_065681.1:p.Val871Gly
|
|