ENST00000282516.13:c.6466T>G
MANE Select
|
ENSP00000282516.8:p.Phe2156Val
|
|
ENST00000652901.1:c.6466T>G
|
ENSP00000499536.1:p.Phe2156Val
|
|
ENST00000282516.12:c.6466T>G
|
ENSP00000282516.8:p.Phe2156Val
|
|
ENST00000448238.2:c.6466T>G
|
ENSP00000406266.2:p.Phe2156Val
|
|
ENST00000621733.1:c.1-19013T>G
|
ENSP00000480694.1:n.1-19013T>G
|
|
NM_015384.4:c.6466T>G
|
NP_056199.2:p.Phe2156Val
|
|
NM_133433.3:c.6466T>G
|
NP_597677.2:p.Phe2156Val
|
|
XM_005248280.2:c.6466T>G
|
XP_005248337.1:p.Phe2156Val
|
|
XM_005248282.3:c.5722T>G
|
XP_005248339.2:p.Phe1908Val
|
|
XM_006714467.2:c.6466T>G
|
XP_006714530.1:p.Phe2156Val
|
|
XM_006714468.1:c.6268T>G
|
XP_006714531.1:p.Phe2090Val
|
|
XM_011514014.1:c.6085T>G
|
XP_011512316.1:p.Phe2029Val
|
|
XM_011514015.1:c.6466T>G
|
XP_011512317.1:p.Phe2156Val
|
|
XM_005248280.3:c.6466T>G
|
XP_005248337.1:p.Phe2156Val
|
|
XM_005248282.5:c.5806T>G
|
XP_005248339.3:p.Phe1936Val
|
|
XM_006714468.2:c.6268T>G
|
XP_006714531.1:p.Phe2090Val
|
|
XM_017009329.1:c.6466T>G
|
XP_016864818.1:p.Phe2156Val
|
|
XM_017009330.2:c.4849T>G
|
XP_016864819.1:p.Phe1617Val
|
|
XM_017009331.1:c.4840T>G
|
XP_016864820.1:p.Phe1614Val
|
|
NM_133433.4:c.6466T>G
MANE Select
|
NP_597677.2:p.Phe2156Val
|
|
NM_015384.5:c.6466T>G
|
NP_056199.2:p.Phe2156Val
|
|