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ENST00000518721.6:c.186+40476_186+40477delinsCT
MANE Select
|
ENSP00000429900.1:n.186+40476_186+40477de...
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ENST00000357668.2:c.165+40476_165+40477delinsCT
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ENSP00000350297.2:n.165+40476_165+40477de...
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ENST00000518721.5:c.186+40476_186+40477delinsCT
|
ENSP00000429900.1:n.186+40476_186+40477de...
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|
|
ENST00000520927.5:c.*168+40476_*168+40477delinsCT
|
ENSP00000428629.1:n.*168+40476_*168+40477...
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ENST00000521075.5:c.*168+40476_*168+40477delinsCT
|
ENSP00000428463.1:n.*168+40476_*168+40477...
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|
ENST00000521426.5:c.165+40476_165+40477delinsCT
|
ENSP00000430917.1:n.165+40476_165+40477de...
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|
ENST00000524299.1:c.*168+40476_*168+40477delinsCT
|
ENSP00000429614.1:n.*168+40476_*168+40477...
|
|
|
ENST00000524367.5:n.96+23301_96+23302delinsCT
|
|
|
|
NM_001247996.1:c.165+40476_165+40477delinsCT
|
NP_001234925.1:n.165+40476_165+40477delin...
|
|
|
NM_018482.3:c.186+40476_186+40477delinsCT
|
NP_060952.2:n.186+40476_186+40477delinsCT...
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|
|
XM_005250925.1:c.186+40476_186+40477delinsCT
|
XP_005250982.1:n.186+40476_186+40477delin...
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|
|
XM_006716563.2:c.186+40476_186+40477delinsCT
|
XP_006716626.1:n.186+40476_186+40477delin...
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XM_006716564.1:c.165+40476_165+40477delinsCT
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XP_006716627.1:n.165+40476_165+40477delin...
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|
XM_006716565.2:c.-120-27403_-120-27402delinsCT
|
XP_006716628.1:n.-120-27403_-120-27402del...
|
|
|
XM_006716566.1:c.186+40476_186+40477delinsCT
|
XP_006716629.1:n.186+40476_186+40477delin...
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|
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XM_006716567.2:c.10-80547_10-80546delinsCT
|
XP_006716630.1:n.10-80547_10-80546delinsC...
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|
|
XM_011517052.1:c.186+40476_186+40477delinsCT
|
XP_011515354.1:n.186+40476_186+40477delin...
|
|
|
XM_011517053.1:c.165+40476_165+40477delinsCT
|
XP_011515355.1:n.165+40476_165+40477delin...
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|
|
XR_928643.1:n.2769_2770delinsAG
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XR_928644.1:n.2584_2585delinsAG
|
|
|
|
XR_928645.1:n.2612_2613delinsAG
|
|
|
|
NM_001362924.1:c.186+40476_186+40477delinsCT
|
NP_001349853.1:n.186+40476_186+40477delin...
|
|
|
NM_001362925.1:c.186+40476_186+40477delinsCT
|
NP_001349854.1:n.186+40476_186+40477delin...
|
|
|
NM_001362926.1:c.186+40476_186+40477delinsCT
|
NP_001349855.1:n.186+40476_186+40477delin...
|
|
|
XM_006716563.3:c.186+40476_186+40477delinsCT
|
XP_006716626.1:n.186+40476_186+40477delin...
|
|
|
XM_006716565.3:c.-120-27403_-120-27402delinsCT
|
XP_006716628.1:n.-120-27403_-120-27402del...
|
|
|
XM_011517052.2:c.186+40476_186+40477delinsCT
|
XP_011515354.1:n.186+40476_186+40477delin...
|
|
|
XM_017013467.2:c.51+40141_51+40142delinsCT
|
XP_016868956.1:n.51+40141_51+40142delinsC...
|
|
|
XM_017013468.1:c.10-80547_10-80546delinsCT
|
XP_016868957.1:n.10-80547_10-80546delinsC...
|
|
|
NM_018482.4:c.186+40476_186+40477delinsCT
MANE Select
|
NP_060952.2:n.186+40476_186+40477delinsCT...
|
|
|
NM_001362925.2:c.186+40476_186+40477delinsCT
|
NP_001349854.1:n.186+40476_186+40477delin...
|
|
|
NM_001362926.2:c.186+40476_186+40477delinsCT
|
NP_001349855.1:n.186+40476_186+40477delin...
|
|
|
NM_001247996.2:c.165+40476_165+40477delinsCT
|
NP_001234925.1:n.165+40476_165+40477delin...
|
|
