ENST00000405460.9:c.16351G>C
MANE Select
|
ENSP00000384582.2:p.Glu5451Gln
|
|
ENST00000425867.3:c.5305G>C
|
ENSP00000392618.3:p.Glu1769Gln
|
|
ENST00000638510.1:n.3618G>C
|
|
|
ENST00000639431.1:c.265+147370G>C
|
ENSP00000491057.1:n.265+147370G>C
|
|
ENST00000640061.1:n.128+1397G>C
|
|
|
ENST00000640407.1:c.2761G>C
|
ENSP00000491425.1:p.Glu921Gln
|
|
ENST00000405460.6:c.16351G>C
|
ENSP00000384582.2:p.Glu5451Gln
|
|
ENST00000425867.2:c.3334G>C
|
ENSP00000392618.2:p.Glu1112Gln
|
|
NM_032119.3:c.16351G>C
|
NP_115495.3:p.Glu5451Gln
|
|
NR_003149.1:n.16364G>C
|
|
|
XM_011543675.1:c.16348G>C
|
XP_011541977.1:p.Glu5450Gln
|
|
XM_011543676.1:c.16270G>C
|
XP_011541978.1:p.Glu5424Gln
|
|
XM_011543677.1:c.13654G>C
|
XP_011541979.1:p.Glu4552Gln
|
|
NM_032119.4:c.16351G>C
MANE Select
|
NP_115495.3:p.Glu5451Gln
|
|
XM_017009963.2:c.16372G>C
|
XP_016865452.1:p.Glu5458Gln
|
|
XM_017009964.2:c.16369G>C
|
XP_016865453.1:p.Glu5457Gln
|
|
XM_017009965.1:c.16369G>C
|
XP_016865454.1:p.Glu5457Gln
|
|
XM_017009966.2:c.16291G>C
|
XP_016865455.1:p.Glu5431Gln
|
|
XM_017009967.1:c.16276G>C
|
XP_016865456.1:p.Glu5426Gln
|
|
XM_017009968.2:c.16192G>C
|
XP_016865457.1:p.Glu5398Gln
|
|
XM_017009969.2:c.16372G>C
|
XP_016865458.1:p.Glu5458Gln
|
|
XM_017009972.1:c.9490G>C
|
XP_016865461.1:p.Glu3164Gln
|
|
XM_017009973.1:c.9469G>C
|
XP_016865462.1:p.Glu3157Gln
|
|
NR_003149.2:n.16367G>C
|
|
|