ENST00000433957.7:c.806C>G
|
ENSP00000411013.3:p.Thr269Ser
|
|
ENST00000644384.2:c.806C>G
MANE Select
|
ENSP00000494414.1:p.Thr269Ser
|
|
ENST00000652415.1:c.806C>G
|
ENSP00000498756.1:p.Thr269Ser
|
|
ENST00000291532.7:c.806C>G
|
ENSP00000291532.3:p.Thr269Ser
|
|
ENST00000398397.3:c.806C>G
|
ENSP00000381434.3:p.Thr269Ser
|
|
ENST00000398405.5:c.800C>G
|
ENSP00000381442.1:p.Thr267Ser
|
|
ENST00000433957.6:c.806C>G
|
ENSP00000411013.2:p.Thr269Ser
|
|
ENST00000474596.5:n.674C>G
|
|
|
ENST00000476848.5:n.1541C>G
|
|
|
ENST00000478680.1:n.83C>G
|
|
|
ENST00000482761.1:n.1093C>G
|
|
|
NM_001256317.1:c.806C>G
|
NP_001243246.1:p.Thr269Ser
|
|
NM_024022.2:c.806C>G
|
NP_076927.1:p.Thr269Ser
|
|
NM_032404.2:c.425C>G
|
NP_115780.1:p.Thr142Ser
|
|
NM_032405.1:c.806C>G
|
NP_115781.1:p.Thr269Ser
|
|
NR_046020.1:n.1762C>G
|
|
|
NM_001256317.2:c.806C>G
|
NP_001243246.1:p.Thr269Ser
|
|
NM_024022.3:c.806C>G
|
NP_076927.1:p.Thr269Ser
|
|
NM_032405.2:c.806C>G
|
NP_115781.1:p.Thr269Ser
|
|
NM_001256317.3:c.806C>G
MANE Select
|
NP_001243246.1:p.Thr269Ser
|
|
NM_024022.4:c.806C>G
|
NP_076927.1:p.Thr269Ser
|
|
NM_032404.3:c.425C>G
|
NP_115780.1:p.Thr142Ser
|
|