ENST00000322776.11:c.932G=
MANE Select
|
ENSP00000322450.6:p.Trp311=
|
|
ENST00000647561.1:c.932G=
|
ENSP00000497587.1:p.Trp311=
|
|
ENST00000322776.10:c.932G=
|
ENSP00000322450.6:p.Trp311=
|
|
ENST00000415352.6:c.911G=
|
ENSP00000395368.2:p.Trp304=
|
|
ENST00000526169.1:n.656-101G=
|
|
|
ENST00000526770.5:n.1215G=
|
|
|
ENST00000527355.5:c.221G=
|
ENSP00000432637.1:p.Trp74=
|
|
ENST00000527923.1:n.274G=
|
|
|
ENST00000529927.5:c.905G=
|
ENSP00000436766.1:p.Trp302=
|
|
ENST00000532303.5:c.629G=
|
ENSP00000432015.1:p.Trp210=
|
|
ENST00000533919.5:c.392-56G=
|
ENSP00000435199.1:n.392-56G=
|
|
NM_001166102.1:c.905G=
|
NP_001159574.1:p.Trp302=
|
|
NM_007103.3:c.932G=
|
NP_009034.2:p.Trp311=
|
|
NM_001166102.2:c.905G=
|
NP_001159574.1:p.Trp302=
|
|
NM_007103.4:c.932G=
MANE Select
|
NP_009034.2:p.Trp311=
|
|