ENST00000403665.7:c.1189G>C
MANE Select
|
ENSP00000384957.2:p.Gly397Arg
|
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ENST00000264692.8:c.1027G>C
|
ENSP00000264692.5:p.Gly343Arg
|
|
ENST00000403665.6:c.1189G>C
|
ENSP00000384957.2:p.Gly397Arg
|
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NM_000128.3:c.1189G>C , LRG_583t1:c.1189G>C
|
NP_000119.1:p.Gly397Arg
|
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XM_005262821.2:c.1192G>C
|
XP_005262878.1:p.Gly398Arg
|
|
XM_005262822.2:c.1192G>C
|
XP_005262879.1:p.Gly398Arg
|
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XM_005262823.2:c.922G>C
|
XP_005262880.1:p.Gly308Arg
|
|
XM_005262824.1:c.1192G>C
|
XP_005262881.1:p.Gly398Arg
|
|
XM_006714137.1:c.1144G>C
|
XP_006714200.1:p.Gly382Arg
|
|
XR_938706.1:n.1597G>C
|
|
|
XR_938707.1:n.1597G>C
|
|
|
XM_005262821.4:c.1192G>C
|
XP_005262878.1:p.Gly398Arg
|
|
XM_005262822.4:c.1192G>C
|
XP_005262879.1:p.Gly398Arg
|
|
XM_005262823.4:c.922G>C
|
XP_005262880.1:p.Gly308Arg
|
|
XM_006714137.3:c.1144G>C
|
XP_006714200.1:p.Gly382Arg
|
|
XM_017007884.2:c.*2161G>C
|
XP_016863373.1:n.*2161G>C
|
|
XM_017007885.2:c.*57G>C
|
XP_016863374.1:n.*57G>C
|
|
XR_001741172.2:n.1663G>C
|
|
|
NM_000128.4:c.1189G>C
MANE Select
|
NP_000119.1:p.Gly397Arg
|
|