ENST00000210444.6:c.357T>G
(NANS)
MANE Select
|
ENSP00000210444.5:p.Val119=
|
|
ENST00000210444.5:c.357T>G
(NANS)
|
ENSP00000210444.5:p.Val119=
|
|
ENST00000375098.7:c.*29-7239A>C
(TRIM14)
|
ENSP00000364239.3:n.*29-7239A>C
|
|
ENST00000415280.1:c.-198T>G
(NANS)
|
ENSP00000404107.1:n.-198T>G
|
|
ENST00000461452.1:n.2284T>G
(NANS)
|
|
|
ENST00000495319.1:n.561T>G
(NANS)
|
|
|
NM_018946.3:c.357T>G
(NANS)
|
NP_061819.2:p.Val119=
|
|
XM_011518787.1:c.9T>G
(NANS)
|
XP_011517089.1:p.Val3=
|
|
XM_011518787.2:c.9T>G
(NANS)
|
XP_011517089.1:p.Val3=
|
|
XM_017014811.1:c.-198T>G
(NANS)
|
XP_016870300.1:n.-198T>G
|
|
XM_017015352.2:c.*29-4760A>C
(TRIM14)
|
XP_016870841.1:n.*29-4760A>C
|
|
XM_024447574.1:c.9T>G
(NANS)
|
XP_024303342.1:p.Val3=
|
|
NM_018946.4:c.357T>G
(NANS)
MANE Select
|
NP_061819.2:p.Val119=
|
|