ENST00000370096.9:c.3205G>C
MANE Select
|
ENSP00000359114.3:p.Gly1069Arg
|
|
ENST00000353414.8:c.3088G>C
|
ENSP00000302551.6:p.Gly1030Arg
|
|
ENST00000358392.6:c.3241G>C
|
ENSP00000351163.2:p.Gly1081Arg
|
|
ENST00000370096.7:c.3205G>C
|
ENSP00000359114.3:p.Gly1069Arg
|
|
ENST00000512756.5:c.2857G>C
|
ENSP00000426533.1:p.Gly953Arg
|
|
ENST00000635193.1:c.2539G>C
|
|
|
NM_001190709.1:c.3088G>C
|
NP_001177638.1:p.Gly1030Arg
|
|
NM_001854.3:c.3205G>C
|
NP_001845.3:p.Gly1069Arg
|
|
NM_080629.2:c.3241G>C
|
NP_542196.2:p.Gly1081Arg
|
|
NM_080630.3:c.2857G>C
|
NP_542197.3:p.Gly953Arg
|
|
XM_011540719.1:c.3205G>C
|
XP_011539021.1:p.Gly1069Arg
|
|
XM_011540720.1:c.1438G>C
|
XP_011539022.1:p.Gly480Arg
|
|
XM_011540721.1:c.793G>C
|
XP_011539023.1:p.Gly265Arg
|
|
NR_134980.1:n.3539G>C
|
|
|
XM_017000334.1:c.3358G>C
|
XP_016855823.1:p.Gly1120Arg
|
|
XM_017000335.1:c.3352G>C
|
XP_016855824.1:p.Gly1118Arg
|
|
XM_017000336.1:c.3358G>C
|
XP_016855825.1:p.Gly1120Arg
|
|
XM_017000337.1:c.1756G>C
|
XP_016855826.1:p.Gly586Arg
|
|
NM_001854.4:c.3205G>C
MANE Select
|
NP_001845.3:p.Gly1069Arg
|
|
NM_080630.4:c.2857G>C
|
NP_542197.3:p.Gly953Arg
|
|
NR_134980.2:n.3565G>C
|
|
|
NM_001190709.2:c.3088G>C
|
NP_001177638.1:p.Gly1030Arg
|
|
NM_080629.3:c.3241G>C
|
NP_542196.2:p.Gly1081Arg
|
|