ENST00000682565.1:c.3300G>T
|
ENSP00000507671.1:p.Gln1100His
|
|
ENST00000682801.1:c.3300G>T
|
ENSP00000507862.1:p.Gln1100His
|
|
ENST00000682859.1:c.3300G>T
|
ENSP00000508222.1:p.Gln1100His
|
|
ENST00000683791.1:c.685+17917G>T
|
|
|
ENST00000684460.1:c.752G>T
|
|
|
ENST00000684548.1:c.3300G>T
|
ENSP00000507421.1:p.Gln1100His
|
|
ENST00000684656.1:c.752G>T
|
|
|
ENST00000613296.6:c.3681G>T
MANE Select
|
ENSP00000482968.1:p.Gln1227His
|
|
ENST00000484298.5:c.3555G>T
|
ENSP00000478155.1:p.Gln1185His
|
|
ENST00000613296.4:c.3681G>T
|
ENSP00000482968.1:p.Gln1227His
|
|
ENST00000614410.4:c.3681G>T
|
ENSP00000479094.1:p.Gln1227His
|
|
NM_015120.4:c.3684G>T , LRG_741t1:c.3684G>T
|
NP_055935.4:p.Gln1228His
|
|
NM_001378454.1:c.3681G>T
MANE Select
|
NP_001365383.1:p.Gln1227His
|
|