ENST00000281928.9:c.5123C>G
MANE Select
|
ENSP00000281928.3:p.Thr1708Arg
|
|
ENST00000549786.2:c.4551C>G
|
|
|
ENST00000648379.1:n.3491C>G
|
|
|
ENST00000648737.1:n.4887C>G
|
|
|
ENST00000648825.1:n.1863C>G
|
|
|
ENST00000648916.1:n.3134C>G
|
|
|
ENST00000649146.1:n.2366C>G
|
|
|
ENST00000649607.1:c.3307C>G
|
|
|
ENST00000649775.1:c.1612C>G
|
|
|
ENST00000650226.1:c.5123C>G
|
ENSP00000496981.1:p.Thr1708Arg
|
|
ENST00000281928.7:c.5123C>G
|
ENSP00000281928.3:p.Thr1708Arg
|
|
ENST00000549786.1:c.487C>G
|
|
|
ENST00000552340.1:c.155C>G
|
ENSP00000449876.1:p.Thr52Arg
|
|
NM_015335.4:c.5123C>G
|
NP_056150.1:p.Thr1708Arg
|
|
XM_011538080.1:c.5123C>G
|
XP_011536382.1:p.Thr1708Arg
|
|
XM_011538081.1:c.5120C>G
|
XP_011536383.1:p.Thr1707Arg
|
|
XM_011538082.1:c.5093C>G
|
XP_011536384.1:p.Thr1698Arg
|
|
XM_011538080.2:c.5123C>G
|
XP_011536382.1:p.Thr1708Arg
|
|
XM_011538081.2:c.5120C>G
|
XP_011536383.1:p.Thr1707Arg
|
|
XM_011538082.2:c.5093C>G
|
XP_011536384.1:p.Thr1698Arg
|
|
XM_017019090.1:c.5120C>G
|
XP_016874579.1:p.Thr1707Arg
|
|
NM_015335.5:c.5123C>G
MANE Select
|
NP_056150.1:p.Thr1708Arg
|
|