|
ENST00000703570.1:n.2844+2890G>C
(CARD14)
|
|
|
|
ENST00000326317.11:c.872C>G
(SGSH)
MANE Select
|
ENSP00000314606.6:p.Ala291Gly
|
|
|
ENST00000326317.10:c.872C>G
(SGSH)
|
ENSP00000314606.6:p.Ala291Gly
|
|
|
ENST00000570923.1:c.*82C>G
(SGSH)
|
ENSP00000458200.1:n.*82C>G
|
|
|
ENST00000572257.5:c.474C>G
(SGSH)
|
|
|
|
ENST00000573150.5:c.*82C>G
(SGSH)
|
ENSP00000459280.1:n.*82C>G
|
|
|
ENST00000575282.5:n.2696C>G
(SGSH)
|
|
|
|
ENST00000576856.1:c.71C>G
(SGSH)
|
ENSP00000460720.1:p.Ala24Gly
|
|
|
NM_000199.3:c.872C>G
(SGSH)
|
NP_000190.1:p.Ala291Gly
|
|
|
XM_005257582.2:c.872C>G
(SGSH)
|
XP_005257639.1:p.Ala291Gly
|
|
|
XM_005257583.3:c.872C>G
(SGSH)
|
XP_005257640.1:p.Ala291Gly
|
|
|
XM_011525126.1:c.872C>G
(SGSH)
|
XP_011523428.1:p.Ala291Gly
|
|
|
XM_011525127.1:c.872C>G
(SGSH)
|
XP_011523429.1:p.Ala291Gly
|
|
|
XR_934532.1:n.892C>G
(SGSH)
|
|
|
|
NM_000199.4:c.872C>G
(SGSH)
|
NP_000190.1:p.Ala291Gly
|
|
|
NM_001352921.1:c.872C>G
(SGSH)
|
NP_001339850.1:p.Ala291Gly
|
|
|
NM_001352922.1:c.872C>G
(SGSH)
|
NP_001339851.1:p.Ala291Gly
|
|
|
NR_148201.1:n.853C>G
(SGSH)
|
|
|
|
XM_005257583.4:c.872C>G
(SGSH)
|
XP_005257640.1:p.Ala291Gly
|
|
|
XM_017024952.1:c.872C>G
(SGSH)
|
XP_016880441.1:p.Ala291Gly
|
|
|
XR_001752585.1:n.892C>G
(SGSH)
|
|
|
|
XR_001752586.1:n.892C>G
(SGSH)
|
|
|
|
XR_001752587.1:n.892C>G
(SGSH)
|
|
|
|
XR_001752588.1:n.892C>G
(SGSH)
|
|
|
|
XR_001752589.1:n.892C>G
(SGSH)
|
|
|
|
XR_001752590.1:n.892C>G
(SGSH)
|
|
|
|
XR_001752591.1:n.892C>G
(SGSH)
|
|
|
|
XR_001752592.1:n.892C>G
(SGSH)
|
|
|
|
XR_002958057.1:n.892C>G
(SGSH)
|
|
|
|
XR_934532.2:n.892C>G
(SGSH)
|
|
|
|
NM_000199.5:c.872C>G
(SGSH)
MANE Select
|
NP_000190.1:p.Ala291Gly
|
|
|
NM_001352921.2:c.872C>G
(SGSH)
|
NP_001339850.1:p.Ala291Gly
|
|
|
NM_001352922.2:c.872C>G
(SGSH)
|
NP_001339851.1:p.Ala291Gly
|
|
|
NR_148201.2:n.786C>G
(SGSH)
|
|
|
|
NM_001352921.3:c.872C>G
(SGSH)
|
NP_001339850.1:p.Ala291Gly
|
|
