ENST00000244571.5:c.2882C=
(AARS2)
MANE Select
|
ENSP00000244571.4:p.Ala961=
|
|
ENST00000244571.4:c.2882C=
(AARS2)
|
ENSP00000244571.4:p.Ala961=
|
|
ENST00000438774.2:c.577-6320G=
(TMEM151B)
|
ENSP00000409337.2:n.577-6320G=
|
|
ENST00000491573.1:n.684C=
(AARS2)
|
|
|
ENST00000505802.1:c.314-6320G=
|
|
|
NM_020745.3:c.2882C=
(AARS2)
|
NP_065796.1:p.Ala961=
|
|
XM_005249245.2:c.2591C=
(AARS2)
|
XP_005249302.1:p.Ala864=
|
|
XM_011514764.1:c.2793+533C=
(AARS2)
|
XP_011513066.1:n.2793+533C=
|
|
XR_241907.2:n.2807C=
(AARS2)
|
|
|
XM_005249245.3:c.2591C=
(AARS2)
|
XP_005249302.1:p.Ala864=
|
|
XM_011514764.2:c.2793+533C=
(AARS2)
|
XP_011513066.1:n.2793+533C=
|
|
XM_017011112.1:c.1592C=
(AARS2)
|
XP_016866601.1:p.Ala531=
|
|
NM_020745.4:c.2882C=
(AARS2)
MANE Select
|
NP_065796.2:p.Ala961=
|
|
NM_001318876.2:c.946-141267G=
(POLR1C)
|
NP_001305805.1:n.946-141267G=
|
|