ENST00000698724.1:n.1809G>C
|
|
|
ENST00000698725.1:n.1562G>C
|
|
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ENST00000698726.1:n.3122G>C
|
|
|
ENST00000698727.1:n.2855G>C
|
|
|
ENST00000698728.1:n.3471G>C
|
|
|
ENST00000698729.1:n.4919G>C
|
|
|
ENST00000698730.1:n.5017G>C
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|
|
ENST00000698731.1:c.3751G>C
|
ENSP00000513898.1:p.Gly1251Arg
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|
ENST00000698732.1:c.*2581G>C
|
ENSP00000513899.1:n.*2581G>C
|
|
ENST00000698733.1:c.*3079G>C
|
ENSP00000513900.1:n.*3079G>C
|
|
ENST00000698734.1:c.*2065G>C
|
ENSP00000513901.1:n.*2065G>C
|
|
ENST00000698735.1:n.4243G>C
|
|
|
ENST00000698736.1:n.4656G>C
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|
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ENST00000698737.1:n.4007G>C
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|
|
ENST00000372371.8:c.3892G>C
MANE Select
|
ENSP00000361446.3:p.Gly1298Arg
|
|
ENST00000372371.7:c.3892G>C
|
ENSP00000361446.3:p.Gly1298Arg
|
|
ENST00000616246.4:c.340G>C
|
ENSP00000483738.1:p.Gly114Arg
|
|
NM_007055.3:c.3892G>C
|
NP_008986.2:p.Gly1298Arg
|
|
NM_007055.4:c.3892G>C
MANE Select
|
NP_008986.2:p.Gly1298Arg
|
|