ENST00000266971.8:c.264G>C
MANE Select
|
ENSP00000266971.3:p.Glu88Asp
|
|
ENST00000266971.7:c.264G>C
|
ENSP00000266971.3:p.Glu88Asp
|
|
ENST00000356124.8:c.264G>C
|
ENSP00000348440.4:p.Glu88Asp
|
|
ENST00000394109.7:c.264G>C
|
ENSP00000377668.3:p.Glu88Asp
|
|
ENST00000394115.6:c.264G>C
|
ENSP00000377674.2:p.Glu88Asp
|
|
ENST00000546712.1:n.755G>C
|
|
|
ENST00000546833.5:c.264G>C
|
ENSP00000449872.1:p.Glu88Asp
|
|
ENST00000548274.5:c.264G>C
|
ENSP00000450245.1:p.Glu88Asp
|
|
ENST00000550065.1:c.264G>C
|
ENSP00000450264.1:p.Glu88Asp
|
|
ENST00000550340.5:n.149G>C
|
|
|
ENST00000550478.5:n.343G>C
|
|
|
ENST00000551698.5:n.286G>C
|
|
|
ENST00000551841.6:c.264G>C
|
ENSP00000449443.1:p.Glu88Asp
|
|
ENST00000552258.5:c.264G>C
|
ENSP00000450049.1:p.Glu88Asp
|
|
ENST00000552363.5:n.117G>C
|
|
|
NM_000456.2:c.264G>C
|
NP_000447.2:p.Glu88Asp
|
|
NM_001032386.1:c.264G>C
|
NP_001027558.1:p.Glu88Asp
|
|
NM_001032387.1:c.264G>C
|
NP_001027559.1:p.Glu88Asp
|
|
XM_005269112.1:c.285G>C
|
XP_005269169.1:p.Glu95Asp
|
|
XM_017019905.2:c.285G>C
|
XP_016875394.1:p.Glu95Asp
|
|
XM_017019906.1:c.285G>C
|
XP_016875395.1:p.Glu95Asp
|
|
XM_017019907.2:c.264G>C
|
XP_016875396.1:p.Glu88Asp
|
|
XM_017019908.1:c.264G>C
|
XP_016875397.1:p.Glu88Asp
|
|
XM_024449167.1:c.285G>C
|
XP_024304935.1:p.Glu95Asp
|
|
NM_001032386.2:c.264G>C
MANE Select
|
NP_001027558.1:p.Glu88Asp
|
|
NM_000456.3:c.264G>C
|
NP_000447.2:p.Glu88Asp
|
|
NM_001032387.2:c.264G>C
|
NP_001027559.1:p.Glu88Asp
|
|