|
ENST00000679463.1:c.488C>T
MANE Select
|
ENSP00000505152.1:p.Ala163Val
|
|
|
ENST00000318561.7:c.506C>T
|
ENSP00000316152.3:p.Ala169Val
|
|
|
ENST00000437090.6:c.*133C>T
|
ENSP00000407931.2:n.*133C>T
|
|
|
ENST00000520605.5:c.277-313C>T
|
ENSP00000430266.1:n.277-313C>T
|
|
|
ENST00000521315.5:c.488C>T
|
ENSP00000430410.1:p.Ala163Val
|
|
|
ENST00000522109.5:c.*389C>T
|
ENSP00000429496.1:n.*389C>T
|
|
|
ENST00000523296.1:c.329C>T
|
ENSP00000429619.1:p.Ala110Val
|
|
|
ENST00000524255.5:c.347C>T
|
ENSP00000429552.1:p.Ala116Val
|
|
|
NM_001172357.1:c.488C>T
|
NP_001165828.1:p.Ala163Val
|
|
|
NM_001172410.1:c.506C>T
|
NP_001165881.1:p.Ala169Val
|
|
|
NM_003018.3:c.506C>T
|
NP_003009.2:p.Ala169Val
|
|
|
XM_006716379.2:c.488C>T
|
XP_006716442.1:p.Ala163Val
|
|
|
XM_006716380.2:c.488C>T
|
XP_006716443.1:p.Ala163Val
|
|
|
XM_011544612.1:c.347C>T
|
XP_011542914.1:p.Ala116Val
|
|
|
XM_011544613.1:c.347C>T
|
XP_011542915.1:p.Ala116Val
|
|
|
NM_001317778.1:c.488C>T
|
NP_001304707.1:p.Ala163Val
|
|
|
NM_001317779.1:c.347C>T
|
NP_001304708.1:p.Ala116Val
|
|
|
NM_001317780.1:c.488C>T
|
NP_001304709.1:p.Ala163Val
|
|
|
XM_011544613.3:c.347C>T
|
XP_011542915.1:p.Ala116Val
|
|
|
NM_001172357.2:c.488C>T
|
NP_001165828.1:p.Ala163Val
|
|
|
NM_001172410.2:c.506C>T
|
NP_001165881.1:p.Ala169Val
|
|
|
NM_001317778.2:c.488C>T
MANE Select
|
NP_001304707.1:p.Ala163Val
|
|
|
NM_001317779.2:c.347C>T
|
NP_001304708.1:p.Ala116Val
|
|
|
NM_001317780.2:c.488C>T
|
NP_001304709.1:p.Ala163Val
|
|
|
NM_003018.4:c.506C>T
|
NP_003009.2:p.Ala169Val
|
|
|
NM_001385653.1:c.506C>T
|
NP_001372582.1:p.Ala169Val
|
|
|
NM_001385654.1:c.506C>T
|
NP_001372583.1:p.Ala169Val
|
|
|
NM_001385655.1:c.506C>T
|
NP_001372584.1:p.Ala169Val
|
|
|
NM_001385656.1:c.488C>T
|
NP_001372585.1:p.Ala163Val
|
|
|
NM_001385657.1:c.488C>T
|
NP_001372586.1:p.Ala163Val
|
|
|
NM_001385658.1:c.488C>T
|
NP_001372587.1:p.Ala163Val
|
|
|
NM_001385659.1:c.488C>T
|
NP_001372588.1:p.Ala163Val
|
|
|
NM_001385660.1:c.347C>T
|
NP_001372589.1:p.Ala116Val
|
|
