ENST00000244571.5:c.2598+111_2598+112delinsGT
(AARS2)
MANE Select
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ENSP00000244571.4:n.2598+111_2598+112delinsGT
|
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ENST00000244571.4:c.2598+111_2598+112delinsGT
(AARS2)
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ENSP00000244571.4:n.2598+111_2598+112delinsGT
|
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ENST00000438774.2:c.577-4995_577-4994delinsAC
(TMEM151B)
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ENSP00000409337.2:n.577-4995_577-4994delinsAC
|
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ENST00000505802.1:c.314-4995_314-4994delinsAC
|
|
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NM_020745.3:c.2598+111_2598+112delinsGT
(AARS2)
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NP_065796.1:n.2598+111_2598+112delinsGT
|
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XM_005249245.2:c.2307+111_2307+112delinsGT
(AARS2)
|
XP_005249302.1:n.2307+111_2307+112delinsGT
|
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XM_011514764.1:c.2598+111_2598+112delinsGT
(AARS2)
|
XP_011513066.1:n.2598+111_2598+112delinsGT
|
|
XR_241907.2:n.2523+111_2523+112delinsGT
(AARS2)
|
|
|
XM_005249245.3:c.2307+111_2307+112delinsGT
(AARS2)
|
XP_005249302.1:n.2307+111_2307+112delinsGT
|
|
XM_011514764.2:c.2598+111_2598+112delinsGT
(AARS2)
|
XP_011513066.1:n.2598+111_2598+112delinsGT
|
|
XM_017011112.1:c.1308+111_1308+112delinsGT
(AARS2)
|
XP_016866601.1:n.1308+111_1308+112delinsGT
|
|
NM_020745.4:c.2598+111_2598+112delinsGT
(AARS2)
MANE Select
|
NP_065796.2:n.2598+111_2598+112delinsGT
|
|
NM_001318876.2:c.946-139942_946-139941delinsAC
(POLR1C)
|
NP_001305805.1:n.946-139942_946-139941delinsAC
|
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