ENST00000281928.9:c.5125G>T
MANE Select
|
ENSP00000281928.3:p.Glu1709Ter
|
|
ENST00000549786.2:c.4553G>T
|
|
|
ENST00000648379.1:n.3493G>T
|
|
|
ENST00000648737.1:n.4889G>T
|
|
|
ENST00000648825.1:n.1865G>T
|
|
|
ENST00000648916.1:n.3136G>T
|
|
|
ENST00000649146.1:n.2368G>T
|
|
|
ENST00000649607.1:c.3309G>T
|
|
|
ENST00000649775.1:c.1614G>T
|
|
|
ENST00000650226.1:c.5125G>T
|
ENSP00000496981.1:p.Glu1709Ter
|
|
ENST00000281928.7:c.5125G>T
|
ENSP00000281928.3:p.Glu1709Ter
|
|
ENST00000549786.1:c.489G>T
|
|
|
ENST00000552340.1:c.157G>T
|
ENSP00000449876.1:p.Glu53Ter
|
|
NM_015335.4:c.5125G>T
|
NP_056150.1:p.Glu1709Ter
|
|
XM_011538080.1:c.5125G>T
|
XP_011536382.1:p.Glu1709Ter
|
|
XM_011538081.1:c.5122G>T
|
XP_011536383.1:p.Glu1708Ter
|
|
XM_011538082.1:c.5095G>T
|
XP_011536384.1:p.Glu1699Ter
|
|
XM_011538080.2:c.5125G>T
|
XP_011536382.1:p.Glu1709Ter
|
|
XM_011538081.2:c.5122G>T
|
XP_011536383.1:p.Glu1708Ter
|
|
XM_011538082.2:c.5095G>T
|
XP_011536384.1:p.Glu1699Ter
|
|
XM_017019090.1:c.5122G>T
|
XP_016874579.1:p.Glu1708Ter
|
|
NM_015335.5:c.5125G>T
MANE Select
|
NP_056150.1:p.Glu1709Ter
|
|