ENST00000649865.1:c.3279G>T
|
ENSP00000496919.1:p.Leu1093=
|
|
ENST00000650285.1:c.3282G>T
MANE Select
|
ENSP00000497069.1:p.Leu1094=
|
|
ENST00000268035.10:c.3282G>T
|
ENSP00000268035.6:p.Leu1094=
|
|
ENST00000558762.5:c.3279G>T
|
ENSP00000453007.1:p.Leu1093=
|
|
NM_000875.4:c.3282G>T
|
NP_000866.1:p.Leu1094=
|
|
NM_001291858.1:c.3279G>T
|
NP_001278787.1:p.Leu1093=
|
|
XM_011521513.1:c.3345G>T
|
XP_011519815.1:p.Leu1115=
|
|
XM_011521514.1:c.3345G>T
|
XP_011519816.1:p.Leu1115=
|
|
XM_011521515.1:c.3342G>T
|
XP_011519817.1:p.Leu1114=
|
|
XM_011521516.1:c.2373G>T
|
XP_011519818.1:p.Leu791=
|
|
XM_011521517.1:c.1947G>T
|
XP_011519819.1:p.Leu649=
|
|
XM_011521516.2:c.2373G>T
|
XP_011519818.1:p.Leu791=
|
|
XM_011521517.2:c.1947G>T
|
XP_011519819.1:p.Leu649=
|
|
XM_017022136.1:c.3357G>T
|
XP_016877625.1:p.Leu1119=
|
|
XM_017022137.1:c.3357G>T
|
XP_016877626.1:p.Leu1119=
|
|
XM_017022138.1:c.3354G>T
|
XP_016877627.1:p.Leu1118=
|
|
XM_017022139.1:c.2919G>T
|
XP_016877628.1:p.Leu973=
|
|
XM_024449913.1:c.2373G>T
|
XP_024305681.1:p.Leu791=
|
|
NM_000875.5:c.3282G>T
MANE Select
|
NP_000866.1:p.Leu1094=
|
|
NM_001291858.2:c.3279G>T
|
NP_001278787.1:p.Leu1093=
|
|