ENST00000615310.5:c.867+1253G>A
|
ENSP00000480088.2:n.867+1253G>A
|
|
ENST00000683007.1:n.512G>A
|
|
|
ENST00000340058.6:c.938G>A
|
ENSP00000344798.4:p.Arg313Gln
|
|
ENST00000355710.8:c.938G>A
MANE Select
|
ENSP00000347942.3:p.Arg313Gln
|
|
ENST00000671844.1:c.625+3817G>A
|
ENSP00000500541.1:n.625+3817G>A
|
|
ENST00000672389.1:c.74-4761G>A
|
ENSP00000500252.1:n.74-4761G>A
|
|
ENST00000340058.5:c.938G>A
|
ENSP00000344798.4:p.Arg313Gln
|
|
ENST00000355710.7:c.938G>A
|
ENSP00000347942.3:p.Arg313Gln
|
|
ENST00000479913.1:n.533G>A
|
|
|
ENST00000498820.5:c.74-5653G>A
|
ENSP00000419080.1:n.74-5653G>A
|
|
ENST00000615310.4:c.938G>A
|
ENSP00000480088.1:p.Arg313Gln
|
|
NM_020630.4:c.938G>A , LRG_518t2:c.938G>A
|
NP_065681.1:p.Arg313Gln
|
|
NM_020975.4:c.938G>A , LRG_518t1:c.938G>A
|
NP_066124.1:p.Arg313Gln
|
|
XM_011540027.1:c.938G>A
|
XP_011538329.1:p.Arg313Gln
|
|
NM_001355216.1:c.176G>A
|
NP_001342145.1:p.Arg59Gln
|
|
NM_020630.5:c.938G>A
|
NP_065681.1:p.Arg313Gln
|
|
NM_020975.5:c.938G>A
|
NP_066124.1:p.Arg313Gln
|
|
NM_020975.6:c.938G>A
MANE Select
|
NP_066124.1:p.Arg313Gln
|
|
NM_020630.6:c.938G>A
|
NP_065681.1:p.Arg313Gln
|
|