ENST00000682565.1:c.11719A>G
|
ENSP00000507671.1:p.Arg3907Gly
|
|
ENST00000682801.1:c.11167-763A>G
|
ENSP00000507862.1:n.11167-763A>G
|
|
ENST00000682859.1:c.11719A>G
|
ENSP00000508222.1:p.Arg3907Gly
|
|
ENST00000683791.1:c.4805A>G
|
|
|
ENST00000684460.1:c.9000A>G
|
|
|
ENST00000684548.1:c.11719A>G
|
ENSP00000507421.1:p.Arg3907Gly
|
|
ENST00000684590.1:c.6166A>G
|
ENSP00000507376.1:p.Arg2056Gly
|
|
ENST00000684656.1:c.9184A>G
|
|
|
ENST00000613296.6:c.12100A>G
MANE Select
|
ENSP00000482968.1:p.Arg4034Gly
|
|
ENST00000651057.1:c.2254A>G
|
ENSP00000498504.1:p.Arg752Gly
|
|
ENST00000651434.1:c.3456A>G
|
|
|
ENST00000651750.1:c.1260+541A>G
|
|
|
ENST00000652487.1:c.3271A>G
|
|
|
ENST00000464408.3:n.275A>G
|
|
|
ENST00000484298.5:c.11974A>G
|
ENSP00000478155.1:p.Arg3992Gly
|
|
ENST00000613296.4:c.12100A>G
|
ENSP00000482968.1:p.Arg4034Gly
|
|
ENST00000620466.4:n.5903A>G
|
|
|
NM_015120.4:c.12103A>G , LRG_741t1:c.12103A>G
|
NP_055935.4:p.Arg4035Gly
|
|
NM_001378454.1:c.12100A>G
MANE Select
|
NP_001365383.1:p.Arg4034Gly
|
|