ENST00000682565.1:c.7611C>A
|
ENSP00000507671.1:p.Ile2537=
|
|
ENST00000682801.1:c.7611C>A
|
ENSP00000507862.1:p.Ile2537=
|
|
ENST00000682859.1:c.7611C>A
|
ENSP00000508222.1:p.Ile2537=
|
|
ENST00000683791.1:c.1003C>A
|
|
|
ENST00000684460.1:c.5063C>A
|
|
|
ENST00000684548.1:c.7611C>A
|
ENSP00000507421.1:p.Ile2537=
|
|
ENST00000684590.1:c.2058C>A
|
ENSP00000507376.1:p.Ile686=
|
|
ENST00000684656.1:c.5063C>A
|
|
|
ENST00000613296.6:c.7992C>A
MANE Select
|
ENSP00000482968.1:p.Ile2664=
|
|
ENST00000651434.1:c.896-29824C>A
|
|
|
ENST00000423048.5:c.2823C>A
|
ENSP00000399833.1:p.Ile941=
|
|
ENST00000484298.5:c.7866C>A
|
ENSP00000478155.1:p.Ile2622=
|
|
ENST00000613296.4:c.7992C>A
|
ENSP00000482968.1:p.Ile2664=
|
|
ENST00000614410.4:c.7992C>A
|
ENSP00000479094.1:p.Ile2664=
|
|
ENST00000620466.4:n.1795C>A
|
|
|
NM_015120.4:c.7995C>A , LRG_741t1:c.7995C>A
|
NP_055935.4:p.Ile2665=
|
|
NM_001378454.1:c.7992C>A
MANE Select
|
NP_001365383.1:p.Ile2664=
|
|