ENST00000223051.8:c.1682+13G>A
MANE Select
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ENSP00000223051.3:n.1682+13G>A
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ENST00000223051.7:c.1682+13G>A
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ENSP00000223051.3:n.1682+13G>A
|
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ENST00000431692.5:c.*357+13G>A
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ENSP00000413905.1:n.*357+13G>A
|
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ENST00000462090.5:n.633+13G>A
|
|
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ENST00000462107.1:c.1682+13G>A
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ENSP00000420525.1:n.1682+13G>A
|
|
ENST00000465294.5:n.1517+13G>A
|
|
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ENST00000473374.5:n.755+13G>A
|
|
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ENST00000473963.1:n.711+13G>A
|
|
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ENST00000476304.5:n.1303+13G>A
|
|
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ENST00000490084.5:c.1035+13G>A
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|
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NM_001206855.1:c.1169+13G>A
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NP_001193784.1:n.1169+13G>A
|
|
NM_003227.3:c.1682+13G>A
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NP_003218.2:n.1682+13G>A
|
|
XM_005250553.3:c.1682+13G>A
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XP_005250610.1:n.1682+13G>A
|
|
XM_005250554.3:c.1682+13G>A
|
XP_005250611.1:n.1682+13G>A
|
|
XR_927814.1:n.434-3425C>T
|
|
|
NM_001206855.2:c.1169+13G>A
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NP_001193784.1:n.1169+13G>A
|
|
XM_005250553.4:c.1682+13G>A
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XP_005250610.1:n.1682+13G>A
|
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XM_017012573.1:c.1682+13G>A
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XP_016868062.1:n.1682+13G>A
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NM_003227.4:c.1682+13G>A
MANE Select
|
NP_003218.2:n.1682+13G>A
|
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NM_001206855.3:c.1169+13G>A
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NP_001193784.1:n.1169+13G>A
|
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