ENST00000281928.9:c.2059C>T
MANE Select
|
ENSP00000281928.3:p.Gln687Ter
|
|
ENST00000548743.2:c.2029C>T
|
ENSP00000448553.2:p.Gln677Ter
|
|
ENST00000549786.2:c.1487C>T
|
|
|
ENST00000648737.1:n.1823C>T
|
|
|
ENST00000649607.1:c.246C>T
|
|
|
ENST00000649655.1:n.662C>T
|
|
|
ENST00000649762.1:n.2619C>T
|
|
|
ENST00000650226.1:c.2059C>T
|
ENSP00000496981.1:p.Gln687Ter
|
|
ENST00000650443.1:n.76C>T
|
|
|
ENST00000281928.7:c.2059C>T
|
ENSP00000281928.3:p.Gln687Ter
|
|
ENST00000549755.1:n.1556C>T
|
|
|
NM_015335.4:c.2059C>T
|
NP_056150.1:p.Gln687Ter
|
|
XM_011538080.1:c.2059C>T
|
XP_011536382.1:p.Gln687Ter
|
|
XM_011538081.1:c.2059C>T
|
XP_011536383.1:p.Gln687Ter
|
|
XM_011538082.1:c.2029C>T
|
XP_011536384.1:p.Gln677Ter
|
|
XM_011538080.2:c.2059C>T
|
XP_011536382.1:p.Gln687Ter
|
|
XM_011538081.2:c.2059C>T
|
XP_011536383.1:p.Gln687Ter
|
|
XM_011538082.2:c.2029C>T
|
XP_011536384.1:p.Gln677Ter
|
|
XM_017019090.1:c.2059C>T
|
XP_016874579.1:p.Gln687Ter
|
|
NM_015335.5:c.2059C>T
MANE Select
|
NP_056150.1:p.Gln687Ter
|
|