ENST00000265343.10:c.2602G>T
MANE Select
|
ENSP00000265343.5:p.Glu868Ter
|
|
ENST00000265343.9:c.2602G>T
|
ENSP00000265343.5:p.Glu868Ter
|
|
ENST00000378595.7:c.2602G>T
|
ENSP00000367858.3:p.Glu868Ter
|
|
NM_014423.3:c.2602G>T
|
NP_055238.1:p.Glu868Ter
|
|
XM_005271963.3:c.2602G>T
|
XP_005272020.1:p.Glu868Ter
|
|
XM_005271964.3:c.1468G>T
|
XP_005272021.1:p.Glu490Ter
|
|
XM_006714587.2:c.2515G>T
|
XP_006714650.1:p.Glu839Ter
|
|
XM_005271963.5:c.2602G>T
|
XP_005272020.1:p.Glu868Ter
|
|
XM_005271964.4:c.1468G>T
|
XP_005272021.1:p.Glu490Ter
|
|
XM_006714587.4:c.2515G>T
|
XP_006714650.1:p.Glu839Ter
|
|
NM_014423.4:c.2602G>T
MANE Select
|
NP_055238.1:p.Glu868Ter
|
|