|
NM_003114.5:c.1360G>C
MANE Select
|
NP_003105.2:p.Glu454Gln
|
|
ENST00000388798.7:c.1360G>C
MANE Select
|
ENSP00000373450.3:p.Glu454Gln
|
|
NM_001374321.1:c.1360G>C
|
NP_001361250.1:p.Glu454Gln
|
|
NM_003114.4:c.1360G>C
|
NP_003105.2:p.Glu454Gln
|
|
NM_172218.2:c.1360G>C
|
NP_757367.1:p.Glu454Gln
|
|
NM_172218.3:c.1360G>C
|
NP_757367.1:p.Glu454Gln
|
|
ENST00000251809.4:c.1360G>C
|
ENSP00000251809.3:p.Glu454Gln
|
|
ENST00000388798.6:c.1360G>C
|
ENSP00000373450.2:p.Glu454Gln
|
|
ENST00000523302.1:n.267G>C
|
|
|
XM_011517240.1:c.1360G>C
|
XP_011515542.1:p.Glu454Gln
|
|
XM_011517240.2:c.1360G>C
|
XP_011515542.1:p.Glu454Gln
|
|
XM_011517241.1:c.1360G>C
|
XP_011515543.1:p.Glu454Gln
|
|
XM_011517241.2:c.1360G>C
|
XP_011515543.1:p.Glu454Gln
|
|
XM_011517242.1:c.1360G>C
|
XP_011515544.1:p.Glu454Gln
|
|
XM_011517242.2:c.1360G>C
|
XP_011515544.1:p.Glu454Gln
|
|
XM_011517243.1:c.1360G>C
|
XP_011515545.1:p.Glu454Gln
|
|
XM_011517243.2:c.1360G>C
|
XP_011515545.1:p.Glu454Gln
|
|
XM_011517244.1:c.1360G>C
|
XP_011515546.1:p.Glu454Gln
|
|
XM_011517245.1:c.1360G>C
|
XP_011515547.1:p.Glu454Gln
|
|
XM_011517245.2:c.1360G>C
|
XP_011515547.1:p.Glu454Gln
|
|
XM_017013754.1:c.1465G>C
|
XP_016869243.1:p.Glu489Gln
|
|
XM_017013755.1:c.1024G>C
|
XP_016869244.1:p.Glu342Gln
|
|
XR_001745580.1:n.1446G>C
|
|
|
XR_001745581.1:n.1446G>C
|
|
|
XR_001745582.1:n.1446G>C
|
|
|
XR_001745583.1:n.1446G>C
|
|