ENST00000378823.8:c.2055G>T
MANE Select
|
ENSP00000368100.4:p.Gln685His
|
|
ENST00000638452.2:c.1758G>T
|
ENSP00000492349.2:p.Gln586His
|
|
ENST00000638504.1:n.1663G>T
|
|
|
ENST00000638568.2:c.1758G>T
|
ENSP00000491158.2:p.Gln586His
|
|
ENST00000639899.1:n.2574G>T
|
|
|
ENST00000640655.2:c.1758G>T
|
ENSP00000491596.2:p.Gln586His
|
|
ENST00000651160.1:c.*199G>T
|
ENSP00000498829.1:n.*199G>T
|
|
ENST00000651658.1:n.2598G>T
|
|
|
ENST00000651723.1:c.*2138G>T
|
ENSP00000498237.1:n.*2138G>T
|
|
ENST00000652016.1:c.*272G>T
|
ENSP00000498267.1:n.*272G>T
|
|
ENST00000652485.1:c.2088G>T
|
ENSP00000498973.1:p.Gln696His
|
|
ENST00000378823.7:c.2055G>T
|
ENSP00000368100.4:p.Gln685His
|
|
ENST00000423956.5:c.*241G>T
|
ENSP00000390971.1:n.*241G>T
|
|
ENST00000453394.5:c.1872G>T
|
ENSP00000400049.1:p.Gln624His
|
|
ENST00000496204.1:n.138G>T
|
|
|
ENST00000533482.5:c.*1681G>T
|
ENSP00000431225.1:n.*1681G>T
|
|
NM_005732.3:c.2055G>T
|
NP_005723.2:p.Gln685His
|
|
NM_005732.4:c.2055G>T
MANE Select
|
NP_005723.2:p.Gln685His
|
|