ENST00000244571.5:c.2087T>C
(AARS2)
MANE Select
|
ENSP00000244571.4:p.Met696Thr
|
|
ENST00000244571.4:c.2087T>C
(AARS2)
|
ENSP00000244571.4:p.Met696Thr
|
|
ENST00000438774.2:c.577-3599A>G
(TMEM151B)
|
ENSP00000409337.2:n.577-3599A>G
|
|
ENST00000505802.1:c.314-3599A>G
|
|
|
NM_020745.3:c.2087T>C
(AARS2)
|
NP_065796.1:p.Met696Thr
|
|
XM_005249245.2:c.1796T>C
(AARS2)
|
XP_005249302.1:p.Met599Thr
|
|
XM_011514764.1:c.2087T>C
(AARS2)
|
XP_011513066.1:p.Met696Thr
|
|
XR_241907.2:n.2122T>C
(AARS2)
|
|
|
XM_005249245.3:c.1796T>C
(AARS2)
|
XP_005249302.1:p.Met599Thr
|
|
XM_011514764.2:c.2087T>C
(AARS2)
|
XP_011513066.1:p.Met696Thr
|
|
XM_017011112.1:c.797T>C
(AARS2)
|
XP_016866601.1:p.Met266Thr
|
|
NM_020745.4:c.2087T>C
(AARS2)
MANE Select
|
NP_065796.2:p.Met696Thr
|
|
NM_001318876.2:c.946-138546A>G
(POLR1C)
|
NP_001305805.1:n.946-138546A>G
|
|