ENST00000696217.1:n.445G>C
|
|
|
ENST00000219150.10:c.364G>C
MANE Select
|
ENSP00000219150.6:p.Glu122Gln
|
|
ENST00000219150.9:c.364G>C
|
ENSP00000219150.5:p.Glu122Gln
|
|
ENST00000561815.5:c.472G>C
|
ENSP00000456756.1:p.Glu158Gln
|
|
ENST00000563778.5:c.364G>C
|
ENSP00000456266.1:p.Glu122Gln
|
|
ENST00000564768.1:n.177G>C
|
|
|
ENST00000565497.5:c.364G>C
|
ENSP00000456457.1:p.Glu122Gln
|
|
ENST00000567034.5:n.832G>C
|
|
|
ENST00000568763.1:n.1676G>C
|
|
|
ENST00000568982.5:n.482G>C
|
|
|
ENST00000569203.5:c.364G>C
|
ENSP00000454752.1:p.Glu122Gln
|
|
ENST00000569469.1:n.431+138G>C
|
|
|
ENST00000569970.1:c.364G>C
|
ENSP00000457509.1:p.Glu122Gln
|
|
ENST00000570045.5:c.364G>C
|
ENSP00000455552.1:p.Glu122Gln
|
|
ENST00000570244.5:c.241G>C
|
ENSP00000457332.1:p.Glu81Gln
|
|
NM_001193333.2:c.364G>C
|
NP_001180262.1:p.Glu122Gln
|
|
NM_007074.3:c.364G>C
|
NP_009005.1:p.Glu122Gln
|
|
XM_011545714.1:c.364G>C
|
XP_011544016.1:p.Glu122Gln
|
|
XM_011545714.2:c.364G>C
|
XP_011544016.1:p.Glu122Gln
|
|
XM_017022885.2:c.364G>C
|
XP_016878374.1:p.Glu122Gln
|
|
XM_017022886.1:c.364G>C
|
XP_016878375.1:p.Glu122Gln
|
|
NM_007074.4:c.364G>C
MANE Select
|
NP_009005.1:p.Glu122Gln
|
|
NM_001193333.3:c.364G>C
|
NP_001180262.1:p.Glu122Gln
|
|