ENST00000299106.9:c.503G>A
MANE Select
|
ENSP00000299106.4:p.Arg168Gln
|
|
ENST00000299106.8:c.503G>A
|
ENSP00000299106.4:p.Arg168Gln
|
|
ENST00000441717.3:c.350G>A
|
ENSP00000395742.3:p.Arg117Gln
|
|
ENST00000524969.5:n.567G>A
|
|
|
ENST00000531302.5:n.502G>A
|
|
|
ENST00000532165.1:n.533G>A
|
|
|
ENST00000534549.5:c.323G>A
|
ENSP00000433206.1:p.Arg108Gln
|
|
NM_001205329.1:c.350G>A
|
NP_001192258.1:p.Arg117Gln
|
|
NM_032801.4:c.503G>A
|
NP_116190.3:p.Arg168Gln
|
|
NM_032801.5:c.503G>A
MANE Select
|
NP_116190.3:p.Arg168Gln
|
|
NM_001205329.2:c.350G>A
|
NP_001192258.1:p.Arg117Gln
|
|