NM_012293.3:c.2892C>T
MANE Select
|
NP_036425.1:p.Asn964=
|
ENST00000252804.9:c.2892C>T
MANE Select
|
ENSP00000252804.4:p.Asn964=
|
NM_012293.2:c.2892C>T
|
NP_036425.1:p.Asn964=
|
ENST00000252804.8:c.2892C>T
|
ENSP00000252804.4:p.Asn964=
|
ENST00000478155.5:n.2697-4136C>T
|
|
XM_005264707.2:c.2820C>T
|
XP_005264764.1:p.Asn940=
|
XM_005264707.3:c.2820C>T
|
XP_005264764.1:p.Asn940=
|
XM_011510395.1:c.2703C>T
|
XP_011508697.1:p.Asn901=
|
XM_011510396.1:c.2343C>T
|
XP_011508698.1:p.Asn781=
|
XM_011510397.1:c.2343C>T
|
XP_011508699.1:p.Asn781=
|