ENST00000378823.8:c.3002T>G
MANE Select
|
ENSP00000368100.4:p.Met1001Arg
|
|
ENST00000638452.2:c.2705T>G
|
ENSP00000492349.2:p.Met902Arg
|
|
ENST00000638504.1:n.2610T>G
|
|
|
ENST00000638568.2:c.2705T>G
|
ENSP00000491158.2:p.Met902Arg
|
|
ENST00000639899.1:n.3521T>G
|
|
|
ENST00000640655.2:c.2705T>G
|
ENSP00000491596.2:p.Met902Arg
|
|
ENST00000651723.1:c.*3085T>G
|
ENSP00000498237.1:n.*3085T>G
|
|
ENST00000378823.7:c.3002T>G
|
ENSP00000368100.4:p.Met1001Arg
|
|
ENST00000533482.5:c.*2628T>G
|
ENSP00000431225.1:n.*2628T>G
|
|
NM_005732.3:c.3002T>G
|
NP_005723.2:p.Met1001Arg
|
|
NM_005732.4:c.3002T>G
MANE Select
|
NP_005723.2:p.Met1001Arg
|
|