ENST00000355773.6:c.967A>C
MANE Select
|
ENSP00000348019.5:p.Asn323His
|
|
ENST00000355773.5:c.967A>C
|
ENSP00000348019.5:p.Asn323His
|
|
NM_012434.4:c.967A>C
|
NP_036566.1:p.Asn323His
|
|
XM_005248710.2:c.916A>C
|
XP_005248767.1:p.Asn306His
|
|
XM_005248711.1:c.769A>C
|
XP_005248768.1:p.Asn257His
|
|
XM_011535750.1:c.967A>C
|
XP_011534052.1:p.Asn323His
|
|
NM_012434.5:c.967A>C
MANE Select
|
NP_036566.1:p.Asn323His
|
|
NM_001382629.1:c.736A>C
|
NP_001369558.1:p.Asn246His
|
|
NM_001382630.1:c.967A>C
|
NP_001369559.1:p.Asn323His
|
|
NM_001382631.1:c.988A>C
|
NP_001369560.1:p.Asn330His
|
|
NM_001382632.1:c.880A>C
|
NP_001369561.1:p.Asn294His
|
|
NM_001382633.1:c.967A>C
|
NP_001369562.1:p.Asn323His
|
|
NM_001382634.1:c.820-6368A>C
|
NP_001369563.1:n.820-6368A>C
|
|
NM_001382635.1:c.964A>C
|
NP_001369564.1:p.Asn322His
|
|
NM_001382636.1:c.649A>C
|
NP_001369565.1:p.Asn217His
|
|