NM_021073.4:c.846C>T
MANE Select
|
NP_066551.1:p.Asn282=
|
ENST00000370830.4:c.846C>T
MANE Select
|
ENSP00000359866.3:p.Asn282=
|
NM_001329754.1:c.846C>T
|
NP_001316683.1:p.Asn282=
|
NM_001329754.2:c.846C>T
|
NP_001316683.1:p.Asn282=
|
NM_001329756.1:c.846C>T
|
NP_001316685.1:p.Asn282=
|
NM_001329756.2:c.846C>T
|
NP_001316685.1:p.Asn282=
|
NM_021073.2:c.846C>T
|
NP_066551.1:p.Asn282=
|
NM_021073.3:c.846C>T
|
NP_066551.1:p.Asn282=
|
ENST00000370830.3:c.846C>T
|
ENSP00000359866.3:p.Asn282=
|
XM_005249304.2:c.846C>T
|
XP_005249361.1:p.Asn282=
|
XM_011514816.1:c.846C>T
|
XP_011513118.1:p.Asn282=
|
XM_011514817.1:c.846C>T
|
XP_011513119.1:p.Asn282=
|
XM_011514817.3:c.846C>T
|
XP_011513119.1:p.Asn282=
|