|
NM_001081.4:c.9922T>C
MANE Select
|
NP_001072.2:p.Trp3308Arg
|
|
ENST00000377833.10:c.9922T>C
MANE Select
|
ENSP00000367064.4:p.Trp3308Arg
|
|
NM_001081.3:c.9922T>C , LRG_540t1:c.9922T>C
|
NP_001072.2:p.Trp3308Arg
|
|
ENST00000377833.8:c.9922T>C
|
ENSP00000367064.4:p.Trp3308Arg
|
|
ENST00000649135.1:n.517T>C
|
|
|
XM_011519709.1:c.5908T>C
|
XP_011518011.1:p.Trp1970Arg
|
|
XM_011519709.2:c.5908T>C
|
XP_011518011.1:p.Trp1970Arg
|
|
XM_011519710.1:c.5884T>C
|
XP_011518012.1:p.Trp1962Arg
|
|
XM_011519710.2:c.5884T>C
|
XP_011518012.1:p.Trp1962Arg
|
|
XM_011519711.1:c.5764T>C
|
XP_011518013.1:p.Trp1922Arg
|
|
XM_011519711.3:c.5764T>C
|
XP_011518013.1:p.Trp1922Arg
|