ENST00000682565.1:c.10134T>G
|
ENSP00000507671.1:p.Val3378=
|
|
ENST00000682801.1:c.10134T>G
|
ENSP00000507862.1:p.Val3378=
|
|
ENST00000682859.1:c.10134T>G
|
ENSP00000508222.1:p.Val3378=
|
|
ENST00000683791.1:c.3220T>G
|
|
|
ENST00000684460.1:c.7415T>G
|
|
|
ENST00000684548.1:c.10134T>G
|
ENSP00000507421.1:p.Val3378=
|
|
ENST00000684590.1:c.4581T>G
|
ENSP00000507376.1:p.Val1527=
|
|
ENST00000684656.1:c.7460T>G
|
|
|
ENST00000613296.6:c.10515T>G
MANE Select
|
ENSP00000482968.1:p.Val3505=
|
|
ENST00000651057.1:c.669T>G
|
ENSP00000498504.1:p.Val223=
|
|
ENST00000651434.1:c.1871T>G
|
|
|
ENST00000652487.1:c.1612T>G
|
|
|
ENST00000423048.5:c.4006T>G
|
ENSP00000399833.1:n.4006T>G
|
|
ENST00000484298.5:c.10389T>G
|
ENSP00000478155.1:p.Val3463=
|
|
ENST00000613296.4:c.10515T>G
|
ENSP00000482968.1:p.Val3505=
|
|
ENST00000614410.4:c.10515T>G
|
ENSP00000479094.1:p.Val3505=
|
|
ENST00000620466.4:n.4318T>G
|
|
|
NM_015120.4:c.10518T>G , LRG_741t1:c.10518T>G
|
NP_055935.4:p.Val3506=
|
|
NM_001378454.1:c.10515T>G
MANE Select
|
NP_001365383.1:p.Val3505=
|
|