ENST00000400017.7:c.1077+126_1077+127del
MANE Select
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ENSP00000382895.2:n.1077+126_1077+127del
|
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ENST00000400017.6:c.1077+126_1077+127del
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ENSP00000382895.2:n.1077+126_1077+127del
|
|
ENST00000556336.5:c.996+126_996+127del
|
ENSP00000450445.1:n.996+126_996+127del
|
|
ENST00000557771.5:c.996+126_996+127del
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ENSP00000451219.1:n.996+126_996+127del
|
|
NM_020366.3:c.1077+126_1077+127del
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NP_065099.3:n.1077+126_1077+127del
|
|
XM_011536983.1:c.1044+126_1044+127del
|
XP_011535285.1:n.1044+126_1044+127del
|
|
NM_020366.4:c.1077+126_1077+127del
MANE Select
|
NP_065099.3:n.1077+126_1077+127del
|
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