ENST00000351050.8:c.461+22G>T
(GNAT2)
|
ENSP00000251337.3:n.461+22G>T
|
|
ENST00000679935.1:c.461+22G>T
(GNAT2)
MANE Select
|
ENSP00000505083.1:n.461+22G>T
|
|
ENST00000351050.7:c.461+22G>T
(GNAT2)
|
ENSP00000251337.3:n.461+22G>T
|
|
ENST00000369851.5:c.*16287C>A
(GNAI3)
|
ENSP00000358867.4:n.*16287C>A
|
|
NM_005272.3:c.461+22G>T
(GNAT2)
|
NP_005263.1:n.461+22G>T
|
|
XM_011541264.1:c.461+22G>T
(GNAT2)
|
XP_011539566.1:n.461+22G>T
|
|
XM_011541265.1:c.461+22G>T
(GNAT2)
|
XP_011539567.1:n.461+22G>T
|
|
XM_011541266.1:c.461+22G>T
(GNAT2)
|
XP_011539568.1:n.461+22G>T
|
|
XM_011541264.2:c.461+22G>T
(GNAT2)
|
XP_011539566.1:n.461+22G>T
|
|
NM_001377295.1:c.461+22G>T
(GNAT2)
|
NP_001364224.1:n.461+22G>T
|
|
NM_005272.5:c.461+22G>T
(GNAT2)
|
NP_005263.1:n.461+22G>T
|
|
NM_001377295.2:c.461+22G>T
(GNAT2)
MANE Select
|
NP_001364224.1:n.461+22G>T
|
|
NM_001379232.1:c.461+22G>T
(GNAT2)
|
NP_001366161.1:n.461+22G>T
|
|