ENST00000433957.7:c.266T>G
|
ENSP00000411013.3:p.Ile89Arg
|
|
ENST00000644384.2:c.266T>G
MANE Select
|
ENSP00000494414.1:p.Ile89Arg
|
|
ENST00000652415.1:c.266T>G
|
ENSP00000498756.1:p.Ile89Arg
|
|
ENST00000291532.7:c.266T>G
|
ENSP00000291532.3:p.Ile89Arg
|
|
ENST00000398397.3:c.266T>G
|
ENSP00000381434.3:p.Ile89Arg
|
|
ENST00000398405.5:c.260T>G
|
ENSP00000381442.1:p.Ile87Arg
|
|
ENST00000433957.6:c.266T>G
|
ENSP00000411013.2:p.Ile89Arg
|
|
ENST00000474596.5:n.134T>G
|
|
|
ENST00000482761.1:n.553T>G
|
|
|
NM_001256317.1:c.266T>G
|
NP_001243246.1:p.Ile89Arg
|
|
NM_024022.2:c.266T>G
|
NP_076927.1:p.Ile89Arg
|
|
NM_032404.2:c.-116T>G
|
NP_115780.1:n.-116T>G
|
|
NM_032405.1:c.266T>G
|
NP_115781.1:p.Ile89Arg
|
|
NR_046020.1:n.1222T>G
|
|
|
NM_001256317.2:c.266T>G
|
NP_001243246.1:p.Ile89Arg
|
|
NM_024022.3:c.266T>G
|
NP_076927.1:p.Ile89Arg
|
|
NM_032405.2:c.266T>G
|
NP_115781.1:p.Ile89Arg
|
|
NM_001256317.3:c.266T>G
MANE Select
|
NP_001243246.1:p.Ile89Arg
|
|
NM_024022.4:c.266T>G
|
NP_076927.1:p.Ile89Arg
|
|
NM_032404.3:c.-116T>G
|
NP_115780.1:n.-116T>G
|
|