ENST00000378623.6:c.3729_3730delinsTT
MANE Select
|
ENSP00000367888.1:p.Asn1244Tyr
|
|
ENST00000378623.5:c.3729_3730delinsTT
|
ENSP00000367888.1:p.Asn1244Tyr
|
|
NM_002334.3:c.3729_3730delinsTT
|
NP_002325.2:p.Asn1244Tyr
|
|
XM_011520102.1:c.3942_3943delinsTT
|
XP_011518404.1:p.Asn1315Tyr
|
|
XM_011520103.1:c.2925_2926delinsTT
|
XP_011518405.1:p.Asn976Tyr
|
|
XM_011520104.1:c.1494_1495delinsTT
|
XP_011518406.1:p.Asn499Tyr
|
|
XM_011520103.2:c.2925_2926delinsTT
|
XP_011518405.1:p.Asn976Tyr
|
|
XM_011520104.2:c.1494_1495delinsTT
|
XP_011518406.1:p.Asn499Tyr
|
|
XM_017017734.1:c.3729_3730delinsTT
|
XP_016873223.1:p.Asn1244Tyr
|
|
NM_002334.4:c.3729_3730delinsTT
MANE Select
|
NP_002325.2:p.Asn1244Tyr
|
|