ENST00000367466.4:c.1459G>T
MANE Select
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ENSP00000356436.3:p.Gly487Trp
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ENST00000367466.3:c.1459G>T
|
ENSP00000356436.3:p.Gly487Trp
|
|
NM_001311193.1:c.1279G>T
|
NP_001298122.1:p.Gly427Trp
|
|
NM_024420.2:c.1459G>T
|
NP_077734.1:p.Gly487Trp
|
|
XM_005245267.2:c.1348G>T
|
XP_005245324.1:p.Gly450Trp
|
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XM_011509641.1:c.1480G>T
|
XP_011507943.1:p.Gly494Trp
|
|
XM_011509642.1:c.1459G>T
|
XP_011507944.1:p.Gly487Trp
|
|
XM_011509643.1:c.1459G>T
|
XP_011507945.1:p.Gly487Trp
|
|
XR_921838.1:n.1477+43G>T
|
|
|
XM_005245267.4:c.1474G>T
|
XP_005245324.2:p.Gly492Trp
|
|
XM_011509642.2:c.1459G>T
|
XP_011507944.1:p.Gly487Trp
|
|
NM_001311193.2:c.1279G>T
|
NP_001298122.2:p.Gly427Trp
|
|
NM_024420.3:c.1459G>T
MANE Select
|
NP_077734.2:p.Gly487Trp
|
|