ENST00000682565.1:c.11644C>G
|
ENSP00000507671.1:p.Gln3882Glu
|
|
ENST00000682801.1:c.11167-838C>G
|
ENSP00000507862.1:n.11167-838C>G
|
|
ENST00000682859.1:c.11644C>G
|
ENSP00000508222.1:p.Gln3882Glu
|
|
ENST00000683791.1:c.4730C>G
|
|
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ENST00000684460.1:c.8925C>G
|
|
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ENST00000684548.1:c.11644C>G
|
ENSP00000507421.1:p.Gln3882Glu
|
|
ENST00000684590.1:c.6091C>G
|
ENSP00000507376.1:p.Gln2031Glu
|
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ENST00000684656.1:c.9109C>G
|
|
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ENST00000613296.6:c.12025C>G
MANE Select
|
ENSP00000482968.1:p.Gln4009Glu
|
|
ENST00000651057.1:c.2179C>G
|
ENSP00000498504.1:p.Gln727Glu
|
|
ENST00000651434.1:c.3381C>G
|
|
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ENST00000651750.1:c.1260+466C>G
|
|
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ENST00000652487.1:c.3196C>G
|
|
|
ENST00000464408.3:n.200C>G
|
|
|
ENST00000484298.5:c.11899C>G
|
ENSP00000478155.1:p.Gln3967Glu
|
|
ENST00000613296.4:c.12025C>G
|
ENSP00000482968.1:p.Gln4009Glu
|
|
ENST00000620466.4:n.5828C>G
|
|
|
NM_015120.4:c.12028C>G , LRG_741t1:c.12028C>G
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NP_055935.4:p.Gln4010Glu
|
|
NM_001378454.1:c.12025C>G
MANE Select
|
NP_001365383.1:p.Gln4009Glu
|
|