ENST00000378823.8:c.2873T>C
MANE Select
|
ENSP00000368100.4:p.Met958Thr
|
|
ENST00000638452.2:c.2576T>C
|
ENSP00000492349.2:p.Met859Thr
|
|
ENST00000638504.1:n.2481T>C
|
|
|
ENST00000638568.2:c.2576T>C
|
ENSP00000491158.2:p.Met859Thr
|
|
ENST00000639899.1:n.3392T>C
|
|
|
ENST00000640655.2:c.2576T>C
|
ENSP00000491596.2:p.Met859Thr
|
|
ENST00000651160.1:c.*1017T>C
|
ENSP00000498829.1:n.*1017T>C
|
|
ENST00000651723.1:c.*2956T>C
|
ENSP00000498237.1:n.*2956T>C
|
|
ENST00000378823.7:c.2873T>C
|
ENSP00000368100.4:p.Met958Thr
|
|
ENST00000423956.5:c.*1059T>C
|
ENSP00000390971.1:n.*1059T>C
|
|
ENST00000533482.5:c.*2499T>C
|
ENSP00000431225.1:n.*2499T>C
|
|
NM_005732.3:c.2873T>C
|
NP_005723.2:p.Met958Thr
|
|
NM_005732.4:c.2873T>C
MANE Select
|
NP_005723.2:p.Met958Thr
|
|