ENST00000281928.9:c.5037T>G
MANE Select
|
ENSP00000281928.3:p.Ile1679Met
|
|
ENST00000549786.2:c.4465T>G
|
|
|
ENST00000648379.1:n.3405T>G
|
|
|
ENST00000648737.1:n.4801T>G
|
|
|
ENST00000648825.1:n.1777T>G
|
|
|
ENST00000648916.1:n.3048T>G
|
|
|
ENST00000649146.1:n.2280T>G
|
|
|
ENST00000649607.1:c.3221T>G
|
|
|
ENST00000649775.1:c.1526T>G
|
|
|
ENST00000650226.1:c.5037T>G
|
ENSP00000496981.1:p.Ile1679Met
|
|
ENST00000281928.7:c.5037T>G
|
ENSP00000281928.3:p.Ile1679Met
|
|
ENST00000549786.1:c.401T>G
|
|
|
ENST00000552340.1:c.69T>G
|
ENSP00000449876.1:p.Ile23Met
|
|
NM_015335.4:c.5037T>G
|
NP_056150.1:p.Ile1679Met
|
|
XM_011538080.1:c.5037T>G
|
XP_011536382.1:p.Ile1679Met
|
|
XM_011538081.1:c.5034T>G
|
XP_011536383.1:p.Ile1678Met
|
|
XM_011538082.1:c.5007T>G
|
XP_011536384.1:p.Ile1669Met
|
|
XM_011538080.2:c.5037T>G
|
XP_011536382.1:p.Ile1679Met
|
|
XM_011538081.2:c.5034T>G
|
XP_011536383.1:p.Ile1678Met
|
|
XM_011538082.2:c.5007T>G
|
XP_011536384.1:p.Ile1669Met
|
|
XM_017019090.1:c.5034T>G
|
XP_016874579.1:p.Ile1678Met
|
|
NM_015335.5:c.5037T>G
MANE Select
|
NP_056150.1:p.Ile1679Met
|
|