ENST00000649865.1:c.3193C>T
|
ENSP00000496919.1:p.Leu1065=
|
|
ENST00000650285.1:c.3196C>T
MANE Select
|
ENSP00000497069.1:p.Leu1066=
|
|
ENST00000268035.10:c.3196C>T
|
ENSP00000268035.6:p.Leu1066=
|
|
ENST00000558762.5:c.3193C>T
|
ENSP00000453007.1:p.Leu1065=
|
|
ENST00000560972.1:c.269C>T
|
ENSP00000453180.1:p.Ala90Val
|
|
NM_000875.4:c.3196C>T
|
NP_000866.1:p.Leu1066=
|
|
NM_001291858.1:c.3193C>T
|
NP_001278787.1:p.Leu1065=
|
|
XM_011521513.1:c.3259C>T
|
XP_011519815.1:p.Leu1087=
|
|
XM_011521514.1:c.3259C>T
|
XP_011519816.1:p.Leu1087=
|
|
XM_011521515.1:c.3256C>T
|
XP_011519817.1:p.Leu1086=
|
|
XM_011521516.1:c.2287C>T
|
XP_011519818.1:p.Leu763=
|
|
XM_011521517.1:c.1861C>T
|
XP_011519819.1:p.Leu621=
|
|
XM_011521516.2:c.2287C>T
|
XP_011519818.1:p.Leu763=
|
|
XM_011521517.2:c.1861C>T
|
XP_011519819.1:p.Leu621=
|
|
XM_017022136.1:c.3271C>T
|
XP_016877625.1:p.Leu1091=
|
|
XM_017022137.1:c.3271C>T
|
XP_016877626.1:p.Leu1091=
|
|
XM_017022138.1:c.3268C>T
|
XP_016877627.1:p.Leu1090=
|
|
XM_017022139.1:c.2833C>T
|
XP_016877628.1:p.Leu945=
|
|
XM_024449913.1:c.2287C>T
|
XP_024305681.1:p.Leu763=
|
|
NM_000875.5:c.3196C>T
MANE Select
|
NP_000866.1:p.Leu1066=
|
|
NM_001291858.2:c.3193C>T
|
NP_001278787.1:p.Leu1065=
|
|