ENST00000307363.10:c.1795T>G
MANE Select
|
ENSP00000306920.4:p.Leu599Val
|
|
ENST00000307363.9:c.1795T>G
|
ENSP00000306920.4:p.Leu599Val
|
|
ENST00000307377.12:c.1402T>G
|
ENSP00000305920.8:p.Leu468Val
|
|
ENST00000399402.7:c.1705T>G
|
ENSP00000382333.2:p.Leu569Val
|
|
NM_000404.2:c.1795T>G
|
NP_000395.2:p.Leu599Val
|
|
NM_000404.3:c.1795T>G
|
NP_000395.2:p.Leu599Val
|
|
NM_001079811.1:c.1705T>G
|
NP_001073279.1:p.Leu569Val
|
|
NM_001079811.2:c.1705T>G
|
NP_001073279.1:p.Leu569Val
|
|
NM_001135602.1:c.1402T>G
|
NP_001129074.1:p.Leu468Val
|
|
NM_001135602.2:c.1402T>G
|
NP_001129074.1:p.Leu468Val
|
|
NM_001317040.1:c.1939T>G
|
NP_001303969.1:p.Leu647Val
|
|
NM_000404.4:c.1795T>G
MANE Select
|
NP_000395.3:p.Leu599Val
|
|
NM_001079811.3:c.1705T>G
|
NP_001073279.2:p.Leu569Val
|
|
NM_001135602.3:c.1402T>G
|
NP_001129074.2:p.Leu468Val
|
|
NM_001317040.2:c.1939T>G
|
NP_001303969.2:p.Leu647Val
|
|
NM_001393580.1:c.1734+16772T>G
|
NP_001380509.1:n.1734+16772T>G
|
|