ENST00000355497.10:c.227G=
|
ENSP00000347684.5:p.Trp76=
|
|
ENST00000373474.9:c.227G=
MANE Select
|
ENSP00000362573.3:p.Trp76=
|
|
ENST00000526117.6:c.227G=
|
ENSP00000436930.1:p.Trp76=
|
|
ENST00000355497.9:c.227G=
|
ENSP00000347684.5:p.Trp76=
|
|
ENST00000373474.8:c.227G=
|
ENSP00000362573.3:p.Trp76=
|
|
ENST00000526117.5:c.227G=
|
ENSP00000436930.1:p.Trp76=
|
|
ENST00000561065.1:c.158G=
|
ENSP00000453580.1:p.Trp53=
|
|
NM_001174146.1:c.227G=
|
NP_001167617.1:p.Trp76=
|
|
NM_001174147.1:c.227G=
|
NP_001167618.1:p.Trp76=
|
|
NM_002316.3:c.227G=
|
NP_002307.2:p.Trp76=
|
|
NM_001174146.2:c.227G=
|
NP_001167617.1:p.Trp76=
|
|
NM_001174147.2:c.227G=
MANE Select
|
NP_001167618.1:p.Trp76=
|
|
NM_002316.4:c.227G=
|
NP_002307.2:p.Trp76=
|
|