ENST00000368356.9:c.582C>G
(FDPS)
MANE Select
|
ENSP00000357340.4:p.Ala194=
|
|
ENST00000356657.10:c.582C>G
(FDPS)
|
ENSP00000349078.6:p.Ala194=
|
|
ENST00000368356.8:c.582C>G
(FDPS)
|
ENSP00000357340.4:p.Ala194=
|
|
ENST00000447866.5:c.384C>G
(FDPS)
|
ENSP00000391755.1:p.Ala128=
|
|
ENST00000461507.5:n.548C>G
(FDPS)
|
|
|
ENST00000467076.5:c.384C>G
(FDPS)
|
ENSP00000480142.1:p.Ala128=
|
|
ENST00000468479.5:n.596C>G
(FDPS)
|
|
|
ENST00000470171.5:n.494C>G
(FDPS)
|
|
|
ENST00000471117.5:n.346C>G
(FDPS)
|
|
|
ENST00000474345.5:c.*259C>G
(FDPS)
|
ENSP00000478032.1:n.*259C>G
|
|
ENST00000477057.5:n.477C>G
(FDPS)
|
|
|
ENST00000489003.5:n.478C>G
(FDPS)
|
|
|
ENST00000491013.5:c.582C>G
(FDPS)
|
ENSP00000479557.1:p.Ala194=
|
|
ENST00000492244.5:n.2C>G
(FDPS)
|
|
|
ENST00000492887.5:n.15C>G
(FDPS)
|
|
|
ENST00000495308.5:n.479C>G
(FDPS)
|
|
|
ENST00000611010.4:c.69C>G
(FDPS)
|
ENSP00000483188.1:p.Ala23=
|
|
ENST00000612683.1:c.384C>G
(FDPS)
|
ENSP00000478235.1:p.Ala128=
|
|
NM_001135821.1:c.582C>G
(FDPS)
|
NP_001129293.1:p.Ala194=
|
|
NM_001135822.1:c.384C>G
(FDPS)
|
NP_001129294.1:p.Ala128=
|
|
NM_001242824.1:c.384C>G
(FDPS)
|
NP_001229753.1:p.Ala128=
|
|
NM_001242825.1:c.69C>G
(FDPS)
|
NP_001229754.1:p.Ala23=
|
|
NM_002004.3:c.582C>G
(FDPS)
|
NP_001995.1:p.Ala194=
|
|
XM_005244962.1:c.384C>G
(FDPS)
|
XP_005245019.1:p.Ala128=
|
|
XM_005244963.1:c.384C>G
(FDPS)
|
XP_005245020.1:p.Ala128=
|
|
NR_145424.1:n.627+76G>C
(RUSC1-AS1)
|
|
|
NR_145425.1:n.352+76G>C
(RUSC1-AS1)
|
|
|
XM_024454066.1:c.582C>G
(FDPS)
|
XP_024309834.1:p.Ala194=
|
|
XM_024454070.1:c.582C>G
(FDPS)
|
XP_024309838.1:p.Ala194=
|
|
XM_024454071.1:c.384C>G
(FDPS)
|
XP_024309839.1:p.Ala128=
|
|
XM_024454072.1:c.384C>G
(FDPS)
|
XP_024309840.1:p.Ala128=
|
|
XM_024454073.1:c.384C>G
(FDPS)
|
XP_024309841.1:p.Ala128=
|
|
XM_024454074.1:c.384C>G
(FDPS)
|
XP_024309842.1:p.Ala128=
|
|
XM_024454076.1:c.69C>G
(FDPS)
|
XP_024309844.1:p.Ala23=
|
|
NM_001135821.2:c.582C>G
(FDPS)
|
NP_001129293.1:p.Ala194=
|
|
NM_001135822.2:c.384C>G
(FDPS)
|
NP_001129294.1:p.Ala128=
|
|
NM_001242824.2:c.384C>G
(FDPS)
|
NP_001229753.1:p.Ala128=
|
|
NM_002004.4:c.582C>G
(FDPS)
MANE Select
|
NP_001995.1:p.Ala194=
|
|
NM_001242825.2:c.69C>G
(FDPS)
|
NP_001229754.1:p.Ala23=
|
|
NM_001378424.1:c.384C>G
(FDPS)
|
NP_001365353.1:p.Ala128=
|
|
NM_001378425.1:c.384C>G
(FDPS)
|
NP_001365354.1:p.Ala128=
|
|