ENST00000286657.10:c.1671G>A
MANE Select
|
ENSP00000286657.4:p.Trp557Ter
|
|
ENST00000286657.8:c.1671G>A
|
ENSP00000286657.4:p.Trp557Ter
|
|
ENST00000622135.1:c.1671G>A
|
ENSP00000480055.1:p.Trp557Ter
|
|
NM_014243.2:c.1671G>A
|
NP_055058.2:p.Trp557Ter
|
|
XM_011532421.1:c.1614G>A
|
XP_011530723.1:p.Trp538Ter
|
|
XM_011532422.1:c.1587G>A
|
XP_011530724.1:p.Trp529Ter
|
|
XM_011532423.1:c.1029G>A
|
XP_011530725.1:p.Trp343Ter
|
|
XM_011532424.1:c.939G>A
|
XP_011530726.1:p.Trp313Ter
|
|
XM_011532421.2:c.1614G>A
|
XP_011530723.1:p.Trp538Ter
|
|
XM_011532422.3:c.1587G>A
|
XP_011530724.1:p.Trp529Ter
|
|
NM_014243.3:c.1671G>A
MANE Select
|
NP_055058.2:p.Trp557Ter
|
|