ENST00000377833.10:c.10839T>G
MANE Select
|
ENSP00000367064.4:p.Arg3613=
|
|
ENST00000377833.8:c.10839T>G
|
ENSP00000367064.4:p.Arg3613=
|
|
NM_001081.3:c.10839T>G , LRG_540t1:c.10839T>G
|
NP_001072.2:p.Arg3613=
|
|
XM_011519709.1:c.6825T>G
|
XP_011518011.1:p.Arg2275=
|
|
XM_011519710.1:c.6801T>G
|
XP_011518012.1:p.Arg2267=
|
|
XM_011519711.1:c.6681T>G
|
XP_011518013.1:p.Arg2227=
|
|
XM_011519709.2:c.6825T>G
|
XP_011518011.1:p.Arg2275=
|
|
XM_011519710.2:c.6801T>G
|
XP_011518012.1:p.Arg2267=
|
|
XM_011519711.3:c.6681T>G
|
XP_011518013.1:p.Arg2227=
|
|
NM_001081.4:c.10839T>G
MANE Select
|
NP_001072.2:p.Arg3613=
|
|