ENST00000254108.12:c.936+132G>A
MANE Select
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ENSP00000254108.8:n.936+132G>A
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ENST00000254108.11:c.936+132G>A
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ENSP00000254108.7:n.936+132G>A
|
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ENST00000380244.7:c.933+132G>A
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ENSP00000369594.3:n.933+132G>A
|
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ENST00000474990.5:n.230+132G>A
|
|
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ENST00000487509.6:n.4111+132G>A
|
|
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ENST00000564766.1:n.760+132G>A
|
|
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ENST00000566605.5:c.*109+132G>A
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ENSP00000455073.1:n.*109+132G>A
|
|
ENST00000568685.1:c.939+132G>A
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ENSP00000455282.1:n.939+132G>A
|
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ENST00000568901.2:n.310+132G>A
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|
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NM_001170634.1:c.933+132G>A
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NP_001164105.1:n.933+132G>A
|
|
NM_001170937.1:c.924+132G>A
|
NP_001164408.1:n.924+132G>A
|
|
NM_004960.3:c.936+132G>A , LRG_655t1:c.936+132G>A
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NP_004951.1:n.936+132G>A
|
|
NR_028388.2:n.1006+132G>A
|
|
|
XM_005255233.3:c.321+132G>A
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XP_005255290.1:n.321+132G>A
|
|
XM_011545781.1:c.930+132G>A
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XP_011544083.1:n.930+132G>A
|
|
XM_011545782.1:c.321+132G>A
|
XP_011544084.1:n.321+132G>A
|
|
XM_005255233.5:c.321+132G>A
|
XP_005255290.1:n.321+132G>A
|
|
XM_011545782.2:c.321+132G>A
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XP_011544084.1:n.321+132G>A
|
|
XM_024450221.1:c.927+132G>A
|
XP_024305989.1:n.927+132G>A
|
|
NM_004960.4:c.936+132G>A
MANE Select
|
NP_004951.1:n.936+132G>A
|
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