NM_002334.4:c.3557G=
MANE Select
|
NP_002325.2:p.Trp1186=
|
ENST00000378623.6:c.3557G=
MANE Select
|
ENSP00000367888.1:p.Trp1186=
|
NM_002334.3:c.3557G=
|
NP_002325.2:p.Trp1186=
|
ENST00000378623.5:c.3557G=
|
ENSP00000367888.1:p.Trp1186=
|
XM_011520102.1:c.3770G=
|
XP_011518404.1:p.Trp1257=
|
XM_011520103.1:c.2753G=
|
XP_011518405.1:p.Trp918=
|
XM_011520103.2:c.2753G=
|
XP_011518405.1:p.Trp918=
|
XM_011520104.1:c.1322G=
|
XP_011518406.1:p.Trp441=
|
XM_011520104.2:c.1322G=
|
XP_011518406.1:p.Trp441=
|
XM_017017734.1:c.3557G=
|
XP_016873223.1:p.Trp1186=
|