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ENST00000635913.2:c.1944+16564_1944+16571delinsTCTCCCTG
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ENSP00000490425.2:n.1944+16564_1944+16571...
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|
|
ENST00000398814.8:c.1290+16564_1290+16571delinsTCTCCCTG
MANE Select
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ENSP00000381795.3:n.1290+16564_1290+16571...
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|
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ENST00000398814.7:c.1290+16564_1290+16571delinsTCTCCCTG
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ENSP00000381795.3:n.1290+16564_1290+16571...
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|
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ENST00000558659.5:c.931+16564_931+16571delinsTCTCCCTG
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|
|
|
NM_025055.4:c.1290+16564_1290+16571delinsTCTCCCTG
|
NP_079331.3:n.1290+16564_1290+16571delins...
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|
|
XM_005254692.1:c.1290+16564_1290+16571delinsTCTCCCTG
|
XP_005254749.1:n.1290+16564_1290+16571del...
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|
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XM_006720697.2:c.1962+16564_1962+16571delinsTCTCCCTG
|
XP_006720760.1:n.1962+16564_1962+16571del...
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|
|
XM_011522085.1:c.1944+16564_1944+16571delinsTCTCCCTG
|
XP_011520387.1:n.1944+16564_1944+16571del...
|
|
|
XM_011522086.1:c.1308+16564_1308+16571delinsTCTCCCTG
|
XP_011520388.1:n.1308+16564_1308+16571del...
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|
|
XM_011522087.1:c.1290+16564_1290+16571delinsTCTCCCTG
|
XP_011520389.1:n.1290+16564_1290+16571del...
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|
|
XM_011522088.1:c.1290+16564_1290+16571delinsTCTCCCTG
|
XP_011520390.1:n.1290+16564_1290+16571del...
|
|
|
XM_011522089.1:c.402+16564_402+16571delinsTCTCCCTG
|
XP_011520391.1:n.402+16564_402+16571delin...
|
|
|
XM_005254692.2:c.1290+16564_1290+16571delinsTCTCCCTG
|
XP_005254749.1:n.1290+16564_1290+16571del...
|
|
|
XM_011522085.3:c.1944+16564_1944+16571delinsTCTCCCTG
|
XP_011520387.1:n.1944+16564_1944+16571del...
|
|
|
XM_011522087.2:c.1290+16564_1290+16571delinsTCTCCCTG
|
XP_011520389.1:n.1290+16564_1290+16571del...
|
|
|
XM_011522089.3:c.402+16564_402+16571delinsTCTCCCTG
|
XP_011520391.1:n.402+16564_402+16571delin...
|
|
|
XM_017022623.1:c.1944+16564_1944+16571delinsTCTCCCTG
|
XP_016878112.1:n.1944+16564_1944+16571del...
|
|
|
XM_017022624.1:c.1944+16564_1944+16571delinsTCTCCCTG
|
XP_016878113.1:n.1944+16564_1944+16571del...
|
|
|
XM_017022625.1:c.1944+16564_1944+16571delinsTCTCCCTG
|
XP_016878114.1:n.1944+16564_1944+16571del...
|
|
|
XM_017022626.2:c.1944+16564_1944+16571delinsTCTCCCTG
|
XP_016878115.1:n.1944+16564_1944+16571del...
|
|
|
XM_017022627.1:c.1944+16564_1944+16571delinsTCTCCCTG
|
XP_016878116.1:n.1944+16564_1944+16571del...
|
|
|
XM_017022628.1:c.1944+16564_1944+16571delinsTCTCCCTG
|
XP_016878117.1:n.1944+16564_1944+16571del...
|
|
|
XR_001751400.1:n.2566+16564_2566+16571delinsTCTCCCTG
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|
|
|
XR_001751401.1:n.2566+16564_2566+16571delinsTCTCCCTG
|
|
|
|
NM_025055.5:c.1290+16564_1290+16571delinsTCTCCCTG
MANE Select
|
NP_079331.3:n.1290+16564_1290+16571delins...
|
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