ENST00000370192.8:c.722T=
MANE Select
|
ENSP00000359211.3:p.Val241=
|
|
ENST00000370192.7:c.722T=
|
ENSP00000359211.3:p.Val241=
|
|
ENST00000474241.1:n.486T=
|
|
|
NM_000110.3:c.722T= , LRG_722t1:c.722T=
|
NP_000101.2:p.Val241=
|
|
XM_005270562.3:c.722T=
|
XP_005270619.2:p.Val241=
|
|
XM_006710397.2:c.722T=
|
XP_006710460.1:p.Val241=
|
|
XM_006710397.3:c.722T=
|
XP_006710460.1:p.Val241=
|
|
XM_017000507.1:c.611T=
|
XP_016855996.1:p.Val204=
|
|
XM_017000508.2:c.227T=
|
XP_016855997.1:p.Val76=
|
|
XM_017000509.2:c.227T=
|
XP_016855998.1:p.Val76=
|
|
XM_017000510.1:c.227T=
|
XP_016855999.1:p.Val76=
|
|
NM_000110.4:c.722T=
MANE Select
|
NP_000101.2:p.Val241=
|
|