ENST00000312358.12:c.8298C>T
(SPEG)
MANE Select
|
ENSP00000311684.7:p.Val2766=
|
|
ENST00000312358.11:c.8298C>T
(SPEG)
|
ENSP00000311684.7:p.Val2766=
|
|
ENST00000485813.5:n.7541C>T
(SPEG)
|
|
|
NM_005876.4:c.8298C>T
(SPEG)
|
NP_005867.3:p.Val2766=
|
|
XM_005246237.2:c.8016C>T
(SPEG)
|
XP_005246294.1:p.Val2672=
|
|
XM_005246239.2:c.5922C>T
(SPEG)
|
XP_005246296.1:p.Val1974=
|
|
XM_005246240.2:c.5751C>T
(SPEG)
|
XP_005246297.1:p.Val1917=
|
|
XM_005246241.1:c.5751C>T
(SPEG)
|
XP_005246298.1:p.Val1917=
|
|
XM_005246242.3:c.5937C>T
(SPEG)
|
XP_005246299.1:p.Val1979=
|
|
XM_006712189.2:c.7986C>T
(SPEG)
|
XP_006712252.1:p.Val2662=
|
|
XM_006712193.2:c.5751C>T
(SPEG)
|
XP_006712256.1:p.Val1917=
|
|
XM_011510479.1:c.8328C>T
(SPEG)
|
XP_011508781.1:p.Val2776=
|
|
XM_011510480.1:c.8160C>T
(SPEG)
|
XP_011508782.1:p.Val2720=
|
|
XM_011510481.1:c.8151C>T
(SPEG)
|
XP_011508783.1:p.Val2717=
|
|
XM_011510482.1:c.8145C>T
(SPEG)
|
XP_011508784.1:p.Val2715=
|
|
XM_011510483.1:c.8067C>T
(SPEG)
|
XP_011508785.1:p.Val2689=
|
|
XM_011510484.1:c.7983C>T
(SPEG)
|
XP_011508786.1:p.Val2661=
|
|
XR_923921.1:n.353-6793G>A
(ASIC4-AS1)
|
|
|
XM_005246242.4:c.5937C>T
(SPEG)
|
XP_005246299.1:p.Val1979=
|
|
XM_006712189.3:c.7986C>T
(SPEG)
|
XP_006712252.1:p.Val2662=
|
|
XM_006712193.3:c.5751C>T
(SPEG)
|
XP_006712256.1:p.Val1917=
|
|
XM_011510479.2:c.8328C>T
(SPEG)
|
XP_011508781.1:p.Val2776=
|
|
XM_011510483.2:c.8046C>T
(SPEG)
|
XP_011508785.2:p.Val2682=
|
|
XM_017003157.1:c.8046C>T
(SPEG)
|
XP_016858646.1:p.Val2682=
|
|
XM_017003158.2:c.5751C>T
(SPEG)
|
XP_016858647.1:p.Val1917=
|
|
XM_017003160.1:c.3306C>T
(SPEG)
|
XP_016858649.1:p.Val1102=
|
|
XR_923921.2:n.392-6793G>A
(ASIC4-AS1)
|
|
|
NM_005876.5:c.8298C>T
(SPEG)
MANE Select
|
NP_005867.3:p.Val2766=
|
|