|
NM_000147.5:c.882G>C
MANE Select
|
NP_000138.2:p.Glu294Asp
|
|
ENST00000374479.4:c.882G>C
MANE Select
|
ENSP00000363603.3:p.Glu294Asp
|
|
NM_000147.4:c.882G>C
|
NP_000138.2:p.Glu294Asp
|
|
NR_174379.1:n.1060G>C
|
|
|
NR_174380.1:n.1109G>C
|
|
|
NR_174381.1:n.948G>C
|
|
|
NR_174382.1:n.1345G>C
|
|
|
ENST00000374479.3:c.882G>C
|
ENSP00000363603.3:p.Glu294Asp
|
|
XM_005245821.1:c.507G>C
|
XP_005245878.1:p.Glu169Asp
|
|
XM_005245821.3:c.507G>C
|
XP_005245878.1:p.Glu169Asp
|
|
XM_011541167.1:c.249G>C
|
XP_011539469.1:p.Glu83Asp
|
|
XM_011541167.3:c.249G>C
|
XP_011539469.1:p.Glu83Asp
|
|
XM_017000905.2:c.579G>C
|
XP_016856394.1:p.Glu193Asp
|