|
NM_001379270.1:c.105C>A
(CNGA1)
MANE Select
|
NP_001366199.1:p.Cys35Ter
|
|
ENST00000514170.7:c.105C>A
(CNGA1)
MANE Select
|
ENSP00000426862.3:p.Cys35Ter
|
|
NM_000087.3:c.117C>A
(CNGA1)
|
NP_000078.2:p.Cys39Ter
|
|
NM_000087.4:c.117C>A
(CNGA1)
|
NP_000078.2:p.Cys39Ter
|
|
NM_000087.5:c.105C>A
(CNGA1)
|
NP_000078.3:p.Cys35Ter
|
|
NM_001142564.1:c.324C>A
(CNGA1)
|
NP_001136036.1:p.Cys108Ter
|
|
NM_001142564.2:c.105C>A
(CNGA1)
|
NP_001136036.2:p.Cys35Ter
|
|
NM_001375386.1:c.117C>A
(CNGA1)
|
NP_001362315.1:p.Cys39Ter
|
|
NR_125879.1:n.479-6439G>T
|
|
|
ENST00000358519.8:c.117C>A
(CNGA1)
|
ENSP00000351320.4:p.Cys39Ter
|
|
ENST00000402813.7:c.324C>A
(CNGA1)
|
ENSP00000384264.3:p.Cys108Ter
|
|
ENST00000402813.9:c.105C>A
(CNGA1)
|
ENSP00000384264.5:p.Cys35Ter
|
|
ENST00000420489.6:c.117C>A
(CNGA1)
|
ENSP00000389881.2:p.Cys39Ter
|
|
ENST00000420489.7:c.105C>A
(CNGA1)
|
ENSP00000389881.3:p.Cys35Ter
|
|
ENST00000500571.2:n.479-6439G>T
(NIPAL1)
|
|
|
ENST00000504722.5:c.117C>A
(CNGA1)
|
ENSP00000423721.1:p.Cys39Ter
|
|
ENST00000504722.6:c.105C>A
(CNGA1)
|
ENSP00000423721.2:p.Cys35Ter
|
|
ENST00000506118.1:n.105C>A
(CNGA1)
|
|
|
ENST00000513178.1:c.117C>A
(CNGA1)
|
ENSP00000423327.1:p.Cys39Ter
|
|
ENST00000513178.2:c.105C>A
(CNGA1)
|
ENSP00000423327.2:p.Cys35Ter
|
|
ENST00000513724.1:n.563+37881G>T
(NIPAL1)
|
|
|
ENST00000514170.5:c.117C>A
(CNGA1)
|
ENSP00000426862.1:p.Cys39Ter
|
|
ENST00000514520.5:c.117C>A
(CNGA1)
|
ENSP00000421110.1:p.Cys39Ter
|
|
ENST00000514520.6:c.105C>A
(CNGA1)
|
ENSP00000421110.2:p.Cys35Ter
|
|
ENST00000544810.5:c.324C>A
(CNGA1)
|
ENSP00000443401.2:p.Cys108Ter
|
|
XM_005248049.3:c.117C>A
(CNGA1)
|
XP_005248106.1:p.Cys39Ter
|
|
XM_005248049.4:c.342C>A
(CNGA1)
|
XP_005248106.2:p.Cys114Ter
|
|
XM_011513623.1:c.117C>A
(CNGA1)
|
XP_011511925.1:p.Cys39Ter
|
|
XM_011513623.2:c.117C>A
(CNGA1)
|
XP_011511925.1:p.Cys39Ter
|
|
XM_017007712.1:c.117C>A
(CNGA1)
|
XP_016863201.1:p.Cys39Ter
|
