ENST00000374479.4:c.1100A>T
MANE Select
|
ENSP00000363603.3:p.Glu367Val
|
|
ENST00000374479.3:c.1100A>T
|
ENSP00000363603.3:p.Glu367Val
|
|
NM_000147.4:c.1100A>T
|
NP_000138.2:p.Glu367Val
|
|
XM_005245821.1:c.725A>T
|
XP_005245878.1:p.Glu242Val
|
|
XM_011541167.1:c.467A>T
|
XP_011539469.1:p.Glu156Val
|
|
XM_005245821.3:c.725A>T
|
XP_005245878.1:p.Glu242Val
|
|
XM_011541167.3:c.467A>T
|
XP_011539469.1:p.Glu156Val
|
|
XM_017000905.2:c.797A>T
|
XP_016856394.1:p.Glu266Val
|
|
NM_000147.5:c.1100A>T
MANE Select
|
NP_000138.2:p.Glu367Val
|
|
NR_174379.1:n.1278A>T
|
|
|
NR_174380.1:n.1327A>T
|
|
|
NR_174381.1:n.1166A>T
|
|
|
NR_174382.1:n.1563A>T
|
|
|