ENST00000433957.7:c.*466T=
|
ENSP00000411013.3:n.*466T=
|
|
ENST00000644384.2:c.*466T=
MANE Select
|
ENSP00000494414.1:n.*466T=
|
|
ENST00000652415.1:c.*466T=
|
ENSP00000498756.1:n.*466T=
|
|
ENST00000291532.7:c.*466T=
|
ENSP00000291532.3:n.*466T=
|
|
ENST00000398405.5:c.*466T=
|
ENSP00000381442.1:n.*466T=
|
|
ENST00000433957.6:c.*466T=
|
ENSP00000411013.2:n.*466T=
|
|
ENST00000474596.5:n.1699T=
|
|
|
ENST00000476848.5:n.2563T=
|
|
|
ENST00000482761.1:n.2118T=
|
|
|
NM_001256317.1:c.*466T=
|
NP_001243246.1:n.*466T=
|
|
NM_024022.2:c.*466T=
|
NP_076927.1:n.*466T=
|
|
NM_032404.2:c.*466T=
|
NP_115780.1:n.*466T=
|
|
NR_046020.1:n.2787T=
|
|
|
NM_001256317.2:c.*466T=
|
NP_001243246.1:n.*466T=
|
|
NM_024022.3:c.*466T=
|
NP_076927.1:n.*466T=
|
|
NM_001256317.3:c.*466T=
MANE Select
|
NP_001243246.1:n.*466T=
|
|
NM_024022.4:c.*466T=
|
NP_076927.1:n.*466T=
|
|
NM_032404.3:c.*466T=
|
NP_115780.1:n.*466T=
|
|