ENST00000682565.1:c.10296G>T
|
ENSP00000507671.1:p.Val3432=
|
|
ENST00000682801.1:c.10296G>T
|
ENSP00000507862.1:p.Val3432=
|
|
ENST00000682859.1:c.10296G>T
|
ENSP00000508222.1:p.Val3432=
|
|
ENST00000683791.1:c.3382G>T
|
|
|
ENST00000684460.1:c.7577G>T
|
|
|
ENST00000684548.1:c.10296G>T
|
ENSP00000507421.1:p.Val3432=
|
|
ENST00000684590.1:c.4743G>T
|
ENSP00000507376.1:p.Val1581=
|
|
ENST00000684656.1:c.7622G>T
|
|
|
ENST00000613296.6:c.10677G>T
MANE Select
|
ENSP00000482968.1:p.Val3559=
|
|
ENST00000651057.1:c.831G>T
|
ENSP00000498504.1:p.Val277=
|
|
ENST00000651434.1:c.2033G>T
|
|
|
ENST00000651750.1:c.65G>T
|
|
|
ENST00000652487.1:c.1774G>T
|
|
|
ENST00000423048.5:c.4168G>T
|
ENSP00000399833.1:n.4168G>T
|
|
ENST00000484298.5:c.10551G>T
|
ENSP00000478155.1:p.Val3517=
|
|
ENST00000613296.4:c.10677G>T
|
ENSP00000482968.1:p.Val3559=
|
|
ENST00000614410.4:c.10677G>T
|
ENSP00000479094.1:p.Val3559=
|
|
ENST00000620466.4:n.4480G>T
|
|
|
NM_015120.4:c.10680G>T , LRG_741t1:c.10680G>T
|
NP_055935.4:p.Val3560=
|
|
NM_001378454.1:c.10677G>T
MANE Select
|
NP_001365383.1:p.Val3559=
|
|