ENST00000378823.8:c.2509C>T
MANE Select
|
ENSP00000368100.4:p.His837Tyr
|
|
ENST00000638452.2:c.2212C>T
|
ENSP00000492349.2:p.His738Tyr
|
|
ENST00000638504.1:n.2117C>T
|
|
|
ENST00000638568.2:c.2212C>T
|
ENSP00000491158.2:p.His738Tyr
|
|
ENST00000639899.1:n.3028C>T
|
|
|
ENST00000640655.2:c.2212C>T
|
ENSP00000491596.2:p.His738Tyr
|
|
ENST00000651160.1:c.*653C>T
|
ENSP00000498829.1:n.*653C>T
|
|
ENST00000651658.1:n.3052C>T
|
|
|
ENST00000651723.1:c.*2592C>T
|
ENSP00000498237.1:n.*2592C>T
|
|
ENST00000652016.1:c.*726C>T
|
ENSP00000498267.1:n.*726C>T
|
|
ENST00000652485.1:c.2542C>T
|
ENSP00000498973.1:p.His848Tyr
|
|
ENST00000378823.7:c.2509C>T
|
ENSP00000368100.4:p.His837Tyr
|
|
ENST00000423956.5:c.*695C>T
|
ENSP00000390971.1:n.*695C>T
|
|
ENST00000533482.5:c.*2135C>T
|
ENSP00000431225.1:n.*2135C>T
|
|
NM_005732.3:c.2509C>T
|
NP_005723.2:p.His837Tyr
|
|
NM_005732.4:c.2509C>T
MANE Select
|
NP_005723.2:p.His837Tyr
|
|