|
NM_014783.6:c.298-207C>T
(ARHGAP11A)
MANE Select
|
NP_055598.1:n.298-207C>T
|
|
ENST00000361627.8:c.298-207C>T
(ARHGAP11A)
MANE Select
|
ENSP00000355090.3:n.298-207C>T
|
|
NM_001286479.1:c.-270-207C>T
(ARHGAP11A)
|
NP_001273408.1:n.-270-207C>T
|
|
NM_001286479.2:c.-270-207C>T
(ARHGAP11A)
|
NP_001273408.1:n.-270-207C>T
|
|
NM_001286479.3:c.-270-207C>T
(ARHGAP11A)
|
NP_001273408.1:n.-270-207C>T
|
|
NM_001286480.1:c.-270-207C>T
(ARHGAP11A)
|
NP_001273409.1:n.-270-207C>T
|
|
NM_001286480.2:c.-270-207C>T
(ARHGAP11A)
|
NP_001273409.1:n.-270-207C>T
|
|
NM_001286480.3:c.-270-207C>T
(ARHGAP11A)
|
NP_001273409.1:n.-270-207C>T
|
|
NM_001368319.1:c.298-207C>T
(ARHGAP11A-SCG5)
|
NP_001355248.1:n.298-207C>T
|
|
NM_014783.4:c.298-207C>T
(ARHGAP11A)
|
NP_055598.1:n.298-207C>T
|
|
NM_014783.5:c.298-207C>T
(ARHGAP11A)
|
NP_055598.1:n.298-207C>T
|
|
NM_199357.1:c.298-207C>T
(ARHGAP11A)
|
NP_955389.1:n.298-207C>T
|
|
NM_199357.2:c.298-207C>T
(ARHGAP11A)
|
NP_955389.1:n.298-207C>T
|
|
NM_199357.3:c.298-207C>T
(ARHGAP11A)
|
NP_955389.1:n.298-207C>T
|
|
ENST00000361627.7:c.298-207C>T
(ARHGAP11A)
|
ENSP00000355090.3:n.298-207C>T
|
|
ENST00000543522.5:c.-270-207C>T
(ARHGAP11A)
|
ENSP00000440073.1:n.-270-207C>T
|
|
ENST00000563864.5:c.298-207C>T
(ARHGAP11A)
|
ENSP00000456078.1:n.298-207C>T
|
|
ENST00000565905.5:c.-270-207C>T
(ARHGAP11A)
|
ENSP00000455754.1:n.-270-207C>T
|
|
ENST00000567348.5:c.298-207C>T
(ARHGAP11A)
|
ENSP00000454575.1:n.298-207C>T
|
|
ENST00000689909.1:c.292-207C>T
(ARHGAP11A-SCG5)
|
ENSP00000510704.1:n.292-207C>T
|
|
ENST00000692248.1:c.298-207C>T
(ARHGAP11A-SCG5)
|
ENSP00000510771.1:n.298-207C>T
|
|
XM_005254808.3:c.298-207C>T
(ARHGAP11A)
|
XP_005254865.1:n.298-207C>T
|
|
XM_011522260.1:c.298-207C>T
(ARHGAP11A)
|
XP_011520562.1:n.298-207C>T
|
|
XM_011522261.1:c.298-207C>T
(ARHGAP11A)
|
XP_011520563.1:n.298-207C>T
|
|
XM_011522262.1:c.-270-207C>T
(ARHGAP11A)
|
XP_011520564.1:n.-270-207C>T
|
