ENST00000682565.1:c.11641G>T
|
ENSP00000507671.1:p.Gly3881Trp
|
|
ENST00000682801.1:c.11167-841G>T
|
ENSP00000507862.1:n.11167-841G>T
|
|
ENST00000682859.1:c.11641G>T
|
ENSP00000508222.1:p.Gly3881Trp
|
|
ENST00000683791.1:c.4727G>T
|
|
|
ENST00000684460.1:c.8922G>T
|
|
|
ENST00000684548.1:c.11641G>T
|
ENSP00000507421.1:p.Gly3881Trp
|
|
ENST00000684590.1:c.6088G>T
|
ENSP00000507376.1:p.Gly2030Trp
|
|
ENST00000684656.1:c.9106G>T
|
|
|
ENST00000613296.6:c.12022G>T
MANE Select
|
ENSP00000482968.1:p.Gly4008Trp
|
|
ENST00000651057.1:c.2176G>T
|
ENSP00000498504.1:p.Gly726Trp
|
|
ENST00000651434.1:c.3378G>T
|
|
|
ENST00000651750.1:c.1260+463G>T
|
|
|
ENST00000652487.1:c.3193G>T
|
|
|
ENST00000464408.3:n.197G>T
|
|
|
ENST00000484298.5:c.11896G>T
|
ENSP00000478155.1:p.Gly3966Trp
|
|
ENST00000613296.4:c.12022G>T
|
ENSP00000482968.1:p.Gly4008Trp
|
|
ENST00000620466.4:n.5825G>T
|
|
|
NM_015120.4:c.12025G>T , LRG_741t1:c.12025G>T
|
NP_055935.4:p.Gly4009Trp
|
|
NM_001378454.1:c.12022G>T
MANE Select
|
NP_001365383.1:p.Gly4008Trp
|
|