|
NM_022716.4:c.551C>T
MANE Select
|
NP_073207.1:p.Ala184Val
|
|
ENST00000239461.11:c.551C>T
MANE Select
|
ENSP00000239461.6:p.Ala184Val
|
|
NM_006902.4:c.551C>T
|
NP_008833.1:p.Ala184Val
|
|
NM_006902.5:c.551C>T
|
NP_008833.1:p.Ala184Val
|
|
NM_022716.3:c.551C>T
|
NP_073207.1:p.Ala184Val
|
|
ENST00000239461.10:c.551C>T
|
ENSP00000239461.6:p.Ala184Val
|
|
ENST00000367760.7:c.551C>T
|
ENSP00000356734.3:p.Ala184Val
|
|
ENST00000476867.6:n.186C>T
|
|
|
ENST00000495280.5:n.158C>T
|
|
|
ENST00000497230.2:c.551C>T
|
ENSP00000450762.1:p.Ala184Val
|
|
XM_006711388.2:c.410C>T
|
XP_006711451.1:p.Ala137Val
|
|
XM_006711388.3:c.410C>T
|
XP_006711451.1:p.Ala137Val
|