ENST00000305188.13:c.1096G>T
MANE Select
|
ENSP00000306999.8:p.Asp366Tyr
|
|
ENST00000305188.12:c.1096G>T
|
ENSP00000306999.8:p.Asp366Tyr
|
|
ENST00000397418.4:c.40G>T
|
ENSP00000380563.2:p.Asp14Tyr
|
|
ENST00000518262.5:c.210G>T
|
|
|
ENST00000522378.5:c.*71G>T
|
ENSP00000428928.1:n.*71G>T
|
|
NM_001017420.2:c.1096G>T
|
NP_001017420.1:p.Asp366Tyr
|
|
XM_011544421.1:c.1096G>T
|
XP_011542723.1:p.Asp366Tyr
|
|
XM_011544422.1:c.1096G>T
|
XP_011542724.1:p.Asp366Tyr
|
|
XR_949378.1:n.1180G>T
|
|
|
XR_949379.1:n.1180G>T
|
|
|
XM_011544421.2:c.1096G>T
|
XP_011542723.1:p.Asp366Tyr
|
|
XM_011544422.2:c.1096G>T
|
XP_011542724.1:p.Asp366Tyr
|
|
XR_949378.3:n.1180G>T
|
|
|
NM_001017420.3:c.1096G>T
MANE Select
|
NP_001017420.1:p.Asp366Tyr
|
|