ENST00000370096.9:c.2644C>A
MANE Select
|
ENSP00000359114.3:p.Arg882Ser
|
|
ENST00000353414.8:c.2527C>A
|
ENSP00000302551.6:p.Arg843Ser
|
|
ENST00000358392.6:c.2680C>A
|
ENSP00000351163.2:p.Arg894Ser
|
|
ENST00000370096.7:c.2644C>A
|
ENSP00000359114.3:p.Arg882Ser
|
|
ENST00000512756.5:c.2296C>A
|
ENSP00000426533.1:p.Arg766Ser
|
|
ENST00000635193.1:c.1978C>A
|
|
|
NM_001190709.1:c.2527C>A
|
NP_001177638.1:p.Arg843Ser
|
|
NM_001854.3:c.2644C>A
|
NP_001845.3:p.Arg882Ser
|
|
NM_080629.2:c.2680C>A
|
NP_542196.2:p.Arg894Ser
|
|
NM_080630.3:c.2296C>A
|
NP_542197.3:p.Arg766Ser
|
|
XM_011540719.1:c.2644C>A
|
XP_011539021.1:p.Arg882Ser
|
|
XM_011540720.1:c.877C>A
|
XP_011539022.1:p.Arg293Ser
|
|
XM_011540721.1:c.232C>A
|
XP_011539023.1:p.Arg78Ser
|
|
XR_946545.1:n.3058C>A
|
|
|
NR_134980.1:n.2978C>A
|
|
|
XM_017000334.1:c.2797C>A
|
XP_016855823.1:p.Arg933Ser
|
|
XM_017000335.1:c.2791C>A
|
XP_016855824.1:p.Arg931Ser
|
|
XM_017000336.1:c.2797C>A
|
XP_016855825.1:p.Arg933Ser
|
|
XM_017000337.1:c.1195C>A
|
XP_016855826.1:p.Arg399Ser
|
|
NM_001854.4:c.2644C>A
MANE Select
|
NP_001845.3:p.Arg882Ser
|
|
NM_080630.4:c.2296C>A
|
NP_542197.3:p.Arg766Ser
|
|
NR_134980.2:n.3004C>A
|
|
|
NM_001190709.2:c.2527C>A
|
NP_001177638.1:p.Arg843Ser
|
|
NM_080629.3:c.2680C>A
|
NP_542196.2:p.Arg894Ser
|
|