ENST00000433957.7:c.787T>G
|
ENSP00000411013.3:p.Tyr263Asp
|
|
ENST00000644384.2:c.787T>G
MANE Select
|
ENSP00000494414.1:p.Tyr263Asp
|
|
ENST00000652415.1:c.787T>G
|
ENSP00000498756.1:p.Tyr263Asp
|
|
ENST00000291532.7:c.787T>G
|
ENSP00000291532.3:p.Tyr263Asp
|
|
ENST00000398397.3:c.787T>G
|
ENSP00000381434.3:p.Tyr263Asp
|
|
ENST00000398405.5:c.781T>G
|
ENSP00000381442.1:p.Tyr261Asp
|
|
ENST00000433957.6:c.787T>G
|
ENSP00000411013.2:p.Tyr263Asp
|
|
ENST00000474596.5:n.655T>G
|
|
|
ENST00000476848.5:n.1522T>G
|
|
|
ENST00000478680.1:n.64T>G
|
|
|
ENST00000482761.1:n.1074T>G
|
|
|
NM_001256317.1:c.787T>G
|
NP_001243246.1:p.Tyr263Asp
|
|
NM_024022.2:c.787T>G
|
NP_076927.1:p.Tyr263Asp
|
|
NM_032404.2:c.406T>G
|
NP_115780.1:p.Tyr136Asp
|
|
NM_032405.1:c.787T>G
|
NP_115781.1:p.Tyr263Asp
|
|
NR_046020.1:n.1743T>G
|
|
|
NM_001256317.2:c.787T>G
|
NP_001243246.1:p.Tyr263Asp
|
|
NM_024022.3:c.787T>G
|
NP_076927.1:p.Tyr263Asp
|
|
NM_032405.2:c.787T>G
|
NP_115781.1:p.Tyr263Asp
|
|
NM_001256317.3:c.787T>G
MANE Select
|
NP_001243246.1:p.Tyr263Asp
|
|
NM_024022.4:c.787T>G
|
NP_076927.1:p.Tyr263Asp
|
|
NM_032404.3:c.406T>G
|
NP_115780.1:p.Tyr136Asp
|
|