ENST00000366820.10:c.*37T>A
MANE Select
|
ENSP00000355785.5:n.*37T>A
|
|
ENST00000366820.9:c.*37T>A
|
ENSP00000355785.5:n.*37T>A
|
|
ENST00000420304.6:c.*37T>A
|
ENSP00000388009.2:n.*37T>A
|
|
ENST00000616737.1:c.*17T>A
|
ENSP00000484300.1:n.*17T>A
|
|
NM_001172425.1:c.*37T>A
|
NP_001165896.1:n.*37T>A
|
|
NM_003240.3:c.*37T>A
|
NP_003231.2:n.*37T>A
|
|
NM_001172425.2:c.*37T>A
|
NP_001165896.1:n.*37T>A
|
|
NM_003240.4:c.*37T>A
|
NP_003231.2:n.*37T>A
|
|
NM_003240.5:c.*37T>A
MANE Select
|
NP_003231.2:n.*37T>A
|
|
NM_001172425.3:c.*37T>A
|
NP_001165896.1:n.*37T>A
|
|