ENST00000682565.1:c.11614G>C
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ENSP00000507671.1:p.Glu3872Gln
|
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ENST00000682801.1:c.11167-868G>C
|
ENSP00000507862.1:n.11167-868G>C
|
|
ENST00000682859.1:c.11614G>C
|
ENSP00000508222.1:p.Glu3872Gln
|
|
ENST00000683791.1:c.4700G>C
|
|
|
ENST00000684460.1:c.8895G>C
|
|
|
ENST00000684548.1:c.11614G>C
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ENSP00000507421.1:p.Glu3872Gln
|
|
ENST00000684590.1:c.6061G>C
|
ENSP00000507376.1:p.Glu2021Gln
|
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ENST00000684656.1:c.9079G>C
|
|
|
ENST00000613296.6:c.11995G>C
MANE Select
|
ENSP00000482968.1:p.Glu3999Gln
|
|
ENST00000651057.1:c.2149G>C
|
ENSP00000498504.1:p.Glu717Gln
|
|
ENST00000651434.1:c.3351G>C
|
|
|
ENST00000651750.1:c.1260+436G>C
|
|
|
ENST00000652487.1:c.3166G>C
|
|
|
ENST00000464408.3:n.170G>C
|
|
|
ENST00000484298.5:c.11869G>C
|
ENSP00000478155.1:p.Glu3957Gln
|
|
ENST00000613296.4:c.11995G>C
|
ENSP00000482968.1:p.Glu3999Gln
|
|
ENST00000620466.4:n.5798G>C
|
|
|
NM_015120.4:c.11998G>C , LRG_741t1:c.11998G>C
|
NP_055935.4:p.Glu4000Gln
|
|
NM_001378454.1:c.11995G>C
MANE Select
|
NP_001365383.1:p.Glu3999Gln
|
|