ENST00000375412.11:c.743C>T
MANE Select
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ENSP00000364561.5:p.Thr248Ile
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ENST00000649557.1:c.197C>T
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ENSP00000496904.1:p.Thr66Ile
|
|
ENST00000650398.1:n.766C>T
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|
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ENST00000375412.9:c.743C>T
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ENSP00000364561.5:p.Thr248Ile
|
|
ENST00000423591.5:c.197C>T
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ENSP00000414298.1:p.Thr66Ile
|
|
ENST00000428152.1:n.459C>T
|
|
|
ENST00000428378.1:c.194C>T
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ENSP00000416978.1:p.Thr65Ile
|
|
ENST00000476484.5:c.*141C>T
|
ENSP00000429212.1:n.*141C>T
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ENST00000479094.5:n.760C>T
|
|
|
ENST00000483056.5:n.565C>T
|
|
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ENST00000483149.6:n.698C>T
|
|
|
ENST00000520403.1:n.740C>T
|
|
|
ENST00000520470.5:n.819C>T
|
|
|
ENST00000523407.1:n.621C>T
|
|
|
NM_198841.2:c.743C>T
|
NP_942138.2:p.Thr248Ile
|
|
XM_005251736.2:c.830C>T
|
XP_005251793.1:p.Thr277Ile
|
|
NM_001322224.2:c.197C>T
|
NP_001309153.1:p.Thr66Ile
|
|
NM_198841.3:c.743C>T
|
NP_942138.2:p.Thr248Ile
|
|
NR_136229.2:n.1042C>T
|
|
|
NR_136230.2:n.1163C>T
|
|
|
NR_136231.2:n.1756C>T
|
|
|
NR_136232.2:n.968C>T
|
|
|
NR_136233.2:n.791C>T
|
|
|
NR_136234.2:n.825C>T
|
|
|
NR_136235.2:n.847C>T
|
|
|
NR_136236.2:n.1050C>T
|
|
|
NR_136237.2:n.1171C>T
|
|
|
NR_136238.2:n.912C>T
|
|
|
NM_198841.4:c.743C>T
MANE Select
|
NP_942138.2:p.Thr248Ile
|
|
NM_001322224.3:c.197C>T
|
NP_001309153.1:p.Thr66Ile
|
|
NR_136231.3:n.1736C>T
|
|
|
NR_136232.3:n.965C>T
|
|
|
NR_136233.3:n.788C>T
|
|
|
NR_136234.3:n.822C>T
|
|
|
NR_136235.3:n.844C>T
|
|
|
NR_136236.3:n.1047C>T
|
|
|
NR_136237.3:n.1168C>T
|
|
|
NR_136238.3:n.909C>T
|
|
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