ENST00000370096.9:c.2646T>G
MANE Select
|
ENSP00000359114.3:p.Arg882=
|
|
ENST00000353414.8:c.2529T>G
|
ENSP00000302551.6:p.Arg843=
|
|
ENST00000358392.6:c.2682T>G
|
ENSP00000351163.2:p.Arg894=
|
|
ENST00000370096.7:c.2646T>G
|
ENSP00000359114.3:p.Arg882=
|
|
ENST00000512756.5:c.2298T>G
|
ENSP00000426533.1:p.Arg766=
|
|
ENST00000635193.1:c.1980T>G
|
|
|
NM_001190709.1:c.2529T>G
|
NP_001177638.1:p.Arg843=
|
|
NM_001854.3:c.2646T>G
|
NP_001845.3:p.Arg882=
|
|
NM_080629.2:c.2682T>G
|
NP_542196.2:p.Arg894=
|
|
NM_080630.3:c.2298T>G
|
NP_542197.3:p.Arg766=
|
|
XM_011540719.1:c.2646T>G
|
XP_011539021.1:p.Arg882=
|
|
XM_011540720.1:c.879T>G
|
XP_011539022.1:p.Arg293=
|
|
XM_011540721.1:c.234T>G
|
XP_011539023.1:p.Arg78=
|
|
XR_946545.1:n.3060T>G
|
|
|
NR_134980.1:n.2980T>G
|
|
|
XM_017000334.1:c.2799T>G
|
XP_016855823.1:p.Arg933=
|
|
XM_017000335.1:c.2793T>G
|
XP_016855824.1:p.Arg931=
|
|
XM_017000336.1:c.2799T>G
|
XP_016855825.1:p.Arg933=
|
|
XM_017000337.1:c.1197T>G
|
XP_016855826.1:p.Arg399=
|
|
NM_001854.4:c.2646T>G
MANE Select
|
NP_001845.3:p.Arg882=
|
|
NM_080630.4:c.2298T>G
|
NP_542197.3:p.Arg766=
|
|
NR_134980.2:n.3006T>G
|
|
|
NM_001190709.2:c.2529T>G
|
NP_001177638.1:p.Arg843=
|
|
NM_080629.3:c.2682T>G
|
NP_542196.2:p.Arg894=
|
|