ENST00000377833.10:c.7193G>T
MANE Select
|
ENSP00000367064.4:p.Trp2398Leu
|
|
ENST00000377833.8:c.7193G>T
|
ENSP00000367064.4:p.Trp2398Leu
|
|
NM_001081.3:c.7193G>T , LRG_540t1:c.7193G>T
|
NP_001072.2:p.Trp2398Leu
|
|
XM_011519708.1:c.7193G>T
|
XP_011518010.1:p.Trp2398Leu
|
|
XM_011519709.1:c.3179G>T
|
XP_011518011.1:p.Trp1060Leu
|
|
XM_011519710.1:c.3155G>T
|
XP_011518012.1:p.Trp1052Leu
|
|
XM_011519711.1:c.3035G>T
|
XP_011518013.1:p.Trp1012Leu
|
|
XM_011519708.2:c.7193G>T
|
XP_011518010.1:p.Trp2398Leu
|
|
XM_011519709.2:c.3179G>T
|
XP_011518011.1:p.Trp1060Leu
|
|
XM_011519710.2:c.3155G>T
|
XP_011518012.1:p.Trp1052Leu
|
|
XM_011519711.3:c.3035G>T
|
XP_011518013.1:p.Trp1012Leu
|
|
NM_001081.4:c.7193G>T
MANE Select
|
NP_001072.2:p.Trp2398Leu
|
|