ENST00000225964.10:c.4130T=
MANE Select
|
ENSP00000225964.6:p.Met1377=
|
|
ENST00000225964.9:c.4130T=
|
ENSP00000225964.5:p.Met1377=
|
|
ENST00000510710.3:n.1095T=
|
|
|
NM_000088.3:c.4130T= , LRG_1t1:c.4130T=
|
NP_000079.2:p.Met1377=
|
|
XM_005257058.3:c.3860T=
|
XP_005257115.2:p.Met1287=
|
|
XM_005257059.3:c.3212T=
|
XP_005257116.2:p.Met1071=
|
|
XM_011524341.1:c.3932T=
|
XP_011522643.1:p.Met1311=
|
|
XM_005257058.4:c.3860T=
|
XP_005257115.2:p.Met1287=
|
|
XM_005257059.4:c.3212T=
|
XP_005257116.2:p.Met1071=
|
|
NM_000088.4:c.4130T=
MANE Select
|
NP_000079.2:p.Met1377=
|
|