|
ENST00000418658.6:c.2892C>T
(CNTN4)
MANE Select
|
ENSP00000396010.1:p.Phe964=
|
|
|
ENST00000397459.6:c.1908C>T
(CNTN4)
|
ENSP00000380600.2:p.Phe636=
|
|
|
ENST00000397461.5:c.2892C>T
(CNTN4)
|
ENSP00000380602.1:p.Phe964=
|
|
|
ENST00000418658.5:c.2892C>T
(CNTN4)
|
ENSP00000396010.1:p.Phe964=
|
|
|
ENST00000427331.5:c.2892C>T
(CNTN4)
|
ENSP00000413642.1:p.Phe964=
|
|
|
ENST00000484686.1:n.1142C>T
(CNTN4)
|
|
|
|
NM_001206955.1:c.2892C>T
(CNTN4)
|
NP_001193884.1:p.Phe964=
|
|
|
NM_001206956.1:c.1905C>T
(CNTN4)
|
NP_001193885.1:p.Phe635=
|
|
|
NM_175607.2:c.2892C>T
(CNTN4)
|
NP_783200.1:p.Phe964=
|
|
|
NM_175613.2:c.1908C>T
(CNTN4)
|
NP_783302.1:p.Phe636=
|
|
|
NR_046554.1:n.79+7180G>A
(CNTN4-AS1)
|
|
|
|
XM_006713004.2:c.2889C>T
(CNTN4)
|
XP_006713067.1:p.Phe963=
|
|
|
XM_011533425.1:c.2892C>T
(CNTN4)
|
XP_011531727.1:p.Phe964=
|
|
|
XM_011533426.1:c.2892C>T
(CNTN4)
|
XP_011531728.1:p.Phe964=
|
|
|
XM_011533427.1:c.2892C>T
(CNTN4)
|
XP_011531729.1:p.Phe964=
|
|
|
XM_011533428.1:c.2892C>T
(CNTN4)
|
XP_011531730.1:p.Phe964=
|
|
|
XM_011533429.1:c.2892C>T
(CNTN4)
|
XP_011531731.1:p.Phe964=
|
|
|
XM_011533430.1:c.2892C>T
(CNTN4)
|
XP_011531732.1:p.Phe964=
|
|
|
XM_011533431.1:c.2859C>T
(CNTN4)
|
XP_011531733.1:p.Phe953=
|
|
|
NM_001350095.1:c.2892C>T
(CNTN4)
|
NP_001337024.1:p.Phe964=
|
|
|
XM_006713004.4:c.2889C>T
(CNTN4)
|
XP_006713067.1:p.Phe963=
|
|
|
XM_011533425.3:c.2892C>T
(CNTN4)
|
XP_011531727.1:p.Phe964=
|
|
|
XM_011533427.2:c.2892C>T
(CNTN4)
|
XP_011531729.1:p.Phe964=
|
|
|
XM_011533428.2:c.2892C>T
(CNTN4)
|
XP_011531730.1:p.Phe964=
|
|
|
XM_011533429.2:c.2892C>T
(CNTN4)
|
XP_011531731.1:p.Phe964=
|
|
|
XM_011533430.2:c.2892C>T
(CNTN4)
|
XP_011531732.1:p.Phe964=
|
|
|
XM_011533431.2:c.2859C>T
(CNTN4)
|
XP_011531733.1:p.Phe953=
|
|
|
XM_017005782.1:c.2892C>T
(CNTN4)
|
XP_016861271.1:p.Phe964=
|
|
|
XM_017005783.1:c.2892C>T
(CNTN4)
|
XP_016861272.1:p.Phe964=
|
|
|
XM_017005784.2:c.2892C>T
(CNTN4)
|
XP_016861273.1:p.Phe964=
|
|
|
XM_017005785.1:c.2889C>T
(CNTN4)
|
XP_016861274.1:p.Phe963=
|
|
|
XM_017005786.1:c.2889C>T
(CNTN4)
|
XP_016861275.1:p.Phe963=
|
|
|
XM_017005787.1:c.2889C>T
(CNTN4)
|
XP_016861276.1:p.Phe963=
|
|
|
NM_175607.3:c.2892C>T
(CNTN4)
MANE Select
|
NP_783200.1:p.Phe964=
|
|
|
NM_001206955.2:c.2892C>T
(CNTN4)
|
NP_001193884.1:p.Phe964=
|
|
|
NM_001206956.2:c.1905C>T
(CNTN4)
|
NP_001193885.1:p.Phe635=
|
|
|
NM_001350095.2:c.2892C>T
(CNTN4)
|
NP_001337024.1:p.Phe964=
|
|
|
NM_175613.3:c.1908C>T
(CNTN4)
|
NP_783302.1:p.Phe636=
|
|
