ENST00000698724.1:n.1898T>A
|
|
|
ENST00000698725.1:n.1651T>A
|
|
|
ENST00000698726.1:n.3211T>A
|
|
|
ENST00000698727.1:n.2944T>A
|
|
|
ENST00000698728.1:n.3560T>A
|
|
|
ENST00000698729.1:n.5008T>A
|
|
|
ENST00000698730.1:n.5106T>A
|
|
|
ENST00000698731.1:c.3840T>A
|
ENSP00000513898.1:p.His1280Gln
|
|
ENST00000698732.1:c.*2670T>A
|
ENSP00000513899.1:n.*2670T>A
|
|
ENST00000698733.1:c.*3168T>A
|
ENSP00000513900.1:n.*3168T>A
|
|
ENST00000698734.1:c.*2154T>A
|
ENSP00000513901.1:n.*2154T>A
|
|
ENST00000698735.1:n.4332T>A
|
|
|
ENST00000698736.1:n.4745T>A
|
|
|
ENST00000698737.1:n.4096T>A
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|
|
ENST00000372371.8:c.3981T>A
MANE Select
|
ENSP00000361446.3:p.His1327Gln
|
|
ENST00000372371.7:c.3981T>A
|
ENSP00000361446.3:p.His1327Gln
|
|
ENST00000616246.4:c.429T>A
|
ENSP00000483738.1:p.His143Gln
|
|
NM_007055.3:c.3981T>A
|
NP_008986.2:p.His1327Gln
|
|
NM_007055.4:c.3981T>A
MANE Select
|
NP_008986.2:p.His1327Gln
|
|