ENST00000377833.10:c.7192T>G
MANE Select
|
ENSP00000367064.4:p.Trp2398Gly
|
|
ENST00000377833.8:c.7192T>G
|
ENSP00000367064.4:p.Trp2398Gly
|
|
NM_001081.3:c.7192T>G , LRG_540t1:c.7192T>G
|
NP_001072.2:p.Trp2398Gly
|
|
XM_011519708.1:c.7192T>G
|
XP_011518010.1:p.Trp2398Gly
|
|
XM_011519709.1:c.3178T>G
|
XP_011518011.1:p.Trp1060Gly
|
|
XM_011519710.1:c.3154T>G
|
XP_011518012.1:p.Trp1052Gly
|
|
XM_011519711.1:c.3034T>G
|
XP_011518013.1:p.Trp1012Gly
|
|
XM_011519708.2:c.7192T>G
|
XP_011518010.1:p.Trp2398Gly
|
|
XM_011519709.2:c.3178T>G
|
XP_011518011.1:p.Trp1060Gly
|
|
XM_011519710.2:c.3154T>G
|
XP_011518012.1:p.Trp1052Gly
|
|
XM_011519711.3:c.3034T>G
|
XP_011518013.1:p.Trp1012Gly
|
|
NM_001081.4:c.7192T>G
MANE Select
|
NP_001072.2:p.Trp2398Gly
|
|