|
NM_001099287.2:c.703G>C
(NIPAL4)
MANE Select
|
NP_001092757.2:p.Gly235Arg
|
|
ENST00000311946.8:c.703G>C
(NIPAL4)
MANE Select
|
ENSP00000311687.8:p.Gly235Arg
|
|
NM_001099287.1:c.889G>C
(NIPAL4)
|
NP_001092757.1:p.Gly297Arg
|
|
NM_001172292.1:c.832G>C
(NIPAL4)
|
NP_001165763.1:p.Gly278Arg
|
|
ENST00000311946.7:c.889G>C
(NIPAL4)
|
ENSP00000311687.7:p.Gly297Arg
|
|
ENST00000435489.6:c.832G>C
(NIPAL4)
|
ENSP00000406456.2:p.Gly278Arg
|
|
ENST00000435489.7:c.646G>C
(NIPAL4)
|
ENSP00000406456.3:p.Gly216Arg
|
|
ENST00000517951.5:c.*1741+15817C>G
(ADAM19)
|
ENSP00000428376.1:n.*1741+15817C>G
|
|
XM_011534552.1:c.394G>C
(NIPAL4)
|
XP_011532854.1:p.Gly132Arg
|
|
XM_024446043.1:c.190G>C
(NIPAL4)
|
XP_024301811.1:p.Gly64Arg
|