ENST00000433957.7:c.906C>A
|
ENSP00000411013.3:p.Gly302=
|
|
ENST00000644384.2:c.906C>A
MANE Select
|
ENSP00000494414.1:p.Gly302=
|
|
ENST00000652415.1:c.906C>A
|
ENSP00000498756.1:p.Gly302=
|
|
ENST00000291532.7:c.906C>A
|
ENSP00000291532.3:p.Gly302=
|
|
ENST00000398397.3:c.906C>A
|
ENSP00000381434.3:p.Gly302=
|
|
ENST00000398405.5:c.900C>A
|
ENSP00000381442.1:p.Gly300=
|
|
ENST00000433957.6:c.906C>A
|
ENSP00000411013.2:p.Gly302=
|
|
ENST00000474596.5:n.774C>A
|
|
|
ENST00000476848.5:n.1641C>A
|
|
|
ENST00000478680.1:n.183C>A
|
|
|
ENST00000482761.1:n.1193C>A
|
|
|
NM_001256317.1:c.906C>A
|
NP_001243246.1:p.Gly302=
|
|
NM_024022.2:c.906C>A
|
NP_076927.1:p.Gly302=
|
|
NM_032404.2:c.525C>A
|
NP_115780.1:p.Gly175=
|
|
NM_032405.1:c.906C>A
|
NP_115781.1:p.Gly302=
|
|
NR_046020.1:n.1862C>A
|
|
|
NM_001256317.2:c.906C>A
|
NP_001243246.1:p.Gly302=
|
|
NM_024022.3:c.906C>A
|
NP_076927.1:p.Gly302=
|
|
NM_032405.2:c.906C>A
|
NP_115781.1:p.Gly302=
|
|
NM_001256317.3:c.906C>A
MANE Select
|
NP_001243246.1:p.Gly302=
|
|
NM_024022.4:c.906C>A
|
NP_076927.1:p.Gly302=
|
|
NM_032404.3:c.525C>A
|
NP_115780.1:p.Gly175=
|
|