ENST00000433957.7:c.1192C>T
|
ENSP00000411013.3:p.Gln398Ter
|
|
ENST00000644384.2:c.1189C>T
MANE Select
|
ENSP00000494414.1:p.Gln397Ter
|
|
ENST00000652415.1:c.1189C>T
|
ENSP00000498756.1:p.Gln397Ter
|
|
ENST00000291532.7:c.1192C>T
|
ENSP00000291532.3:p.Gln398Ter
|
|
ENST00000398405.5:c.1183C>T
|
ENSP00000381442.1:p.Gln395Ter
|
|
ENST00000433957.6:c.1189C>T
|
ENSP00000411013.2:p.Gln397Ter
|
|
ENST00000474596.5:n.1060C>T
|
|
|
ENST00000476848.5:n.1924C>T
|
|
|
ENST00000482761.1:n.1479C>T
|
|
|
NM_001256317.1:c.1189C>T
|
NP_001243246.1:p.Gln397Ter
|
|
NM_024022.2:c.1192C>T
|
NP_076927.1:p.Gln398Ter
|
|
NM_032404.2:c.811C>T
|
NP_115780.1:p.Gln271Ter
|
|
NR_046020.1:n.2148C>T
|
|
|
NM_001256317.2:c.1189C>T
|
NP_001243246.1:p.Gln397Ter
|
|
NM_024022.3:c.1192C>T
|
NP_076927.1:p.Gln398Ter
|
|
NM_001256317.3:c.1189C>T
MANE Select
|
NP_001243246.1:p.Gln397Ter
|
|
NM_024022.4:c.1192C>T
|
NP_076927.1:p.Gln398Ter
|
|
NM_032404.3:c.811C>T
|
NP_115780.1:p.Gln271Ter
|
|