NM_020812.4:c.5689-322C>T
MANE Select
|
NP_065863.2:n.5689-322C>T
|
ENST00000294618.12:c.5689-322C>T
MANE Select
|
ENSP00000294618.6:n.5689-322C>T
|
NM_001367830.1:c.5794-322C>T
|
NP_001354759.1:n.5794-322C>T
|
NM_020812.3:c.5689-322C>T
|
NP_065863.2:n.5689-322C>T
|
ENST00000294618.11:c.5689-322C>T
|
ENSP00000294618.6:n.5689-322C>T
|
ENST00000586702.1:n.592-322C>T
|
|
ENST00000587656.5:c.3554-322C>T
|
|
ENST00000587656.6:c.5794-322C>T
|
ENSP00000468638.2:n.5794-322C>T
|
ENST00000587734.1:c.75+515C>T
|
ENSP00000468291.1:n.75+515C>T
|
XM_005260000.2:c.5887-322C>T
|
XP_005260057.1:n.5887-322C>T
|
XM_005260001.2:c.5794-322C>T
|
XP_005260058.1:n.5794-322C>T
|
XM_006722804.2:c.3025-322C>T
|
XP_006722867.1:n.3025-322C>T
|
XM_006722804.3:c.3025-322C>T
|
XP_006722867.1:n.3025-322C>T
|
XM_011528150.1:c.5827-322C>T
|
XP_011526452.1:n.5827-322C>T
|
XM_011528151.1:c.5815-322C>T
|
XP_011526453.1:n.5815-322C>T
|
XM_011528152.1:c.5722-322C>T
|
XP_011526454.1:n.5722-322C>T
|
XR_936195.1:n.5934-322C>T
|
|