ENST00000370086.8:c.409G>T
MANE Select
|
ENSP00000359103.3:p.Asp137Tyr
|
|
ENST00000320857.7:c.409G>T
|
ENSP00000317331.3:p.Asp137Tyr
|
|
ENST00000370085.3:c.334G>T
|
ENSP00000359102.3:p.Asp112Tyr
|
|
ENST00000370086.7:c.409G>T
|
ENSP00000359103.3:p.Asp137Tyr
|
|
ENST00000370087.5:c.409G>T
|
ENSP00000359104.1:p.Asp137Tyr
|
|
ENST00000447375.1:n.249G>T
|
|
|
ENST00000460616.5:n.2117G>T
|
|
|
ENST00000471880.5:n.612G>T
|
|
|
ENST00000482902.5:n.2236G>T
|
|
|
ENST00000485612.5:n.524G>T
|
|
|
ENST00000486204.5:n.481G>T
|
|
|
NM_001204526.1:c.442G>T
|
NP_001191455.1:p.Asp148Tyr
|
|
NM_001204527.1:c.433G>T
|
NP_001191456.1:p.Asp145Tyr
|
|
NM_006280.2:c.409G>T
|
NP_006271.1:p.Asp137Tyr
|
|
NR_037927.1:n.754G>T
|
|
|
XM_011531186.1:c.409G>T
|
XP_011529488.1:p.Asp137Tyr
|
|
XM_011531187.1:c.409G>T
|
XP_011529489.1:p.Asp137Tyr
|
|
XM_017029756.1:c.220G>T
|
XP_016885245.1:p.Asp74Tyr
|
|
XM_017029757.1:c.220G>T
|
XP_016885246.1:p.Asp74Tyr
|
|
XM_024452428.1:c.220G>T
|
XP_024308196.1:p.Asp74Tyr
|
|
NM_001204527.2:c.433G>T
|
NP_001191456.1:p.Asp145Tyr
|
|
NM_006280.3:c.409G>T
MANE Select
|
NP_006271.1:p.Asp137Tyr
|
|