NM_020829.4:c.1367G>A
MANE Select
|
NP_065880.2:p.Arg456Gln
|
ENST00000414202.7:c.1367G>A
MANE Select
|
ENSP00000416696.2:p.Arg456Gln
|
NM_001135920.2:c.1367G>A
|
NP_001129392.2:p.Arg456Gln
|
NM_001135920.3:c.1367G>A
|
NP_001129392.2:p.Arg456Gln
|
NM_001135920.4:c.1367G>A
|
NP_001129392.2:p.Arg456Gln
|
NM_001206557.1:c.1367G>A
|
NP_001193486.1:p.Arg456Gln
|
NM_001206557.2:c.1367G>A
|
NP_001193486.1:p.Arg456Gln
|
NM_020829.3:c.1367G>A
|
NP_065880.2:p.Arg456Gln
|
ENST00000251879.10:c.1367G>A
|
ENSP00000251879.6:p.Arg456Gln
|
ENST00000276898.3:n.2086G>A
|
|
ENST00000414202.6:c.1367G>A
|
ENSP00000416696.2:p.Arg456Gln
|
ENST00000418622.7:c.1367G>A
|
ENSP00000402240.4:p.Arg456Gln
|
ENST00000545641.5:c.1152G>A
|
|
XM_005251523.2:c.1364G>A
|
XP_005251580.1:p.Arg455Gln
|
XM_005251523.3:c.1364G>A
|
XP_005251580.1:p.Arg455Gln
|
XM_011517967.1:c.434G>A
|
XP_011516269.1:p.Arg145Gln
|
XM_011517967.2:c.434G>A
|
XP_011516269.1:p.Arg145Gln
|
XM_017014934.1:c.1022G>A
|
XP_016870423.1:p.Arg341Gln
|
XM_017014935.1:c.1022G>A
|
XP_016870424.1:p.Arg341Gln
|
XM_017014936.1:c.1022G>A
|
XP_016870425.1:p.Arg341Gln
|
XR_428426.2:n.1647G>A
|
|
XR_428426.3:n.1647G>A
|
|