ENST00000545968.6:c.2842_2843del
MANE Select
|
ENSP00000442795.1:p.Asn948TyrfsTer?
|
|
ENST00000256993.8:c.2842_2843del
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ENSP00000256993.5:p.Asn948TyrfsTer?
|
|
ENST00000399249.6:c.2842_2843del
|
ENSP00000382193.2:p.Asn948TyrfsTer?
|
|
ENST00000545968.5:c.2842_2843del
|
ENSP00000442795.1:p.Asn948TyrfsTer?
|
|
NM_000256.3:c.2842_2843del , LRG_386t1:c.2842_2843del
MANE Select
|
NP_000247.2:p.Asn948TyrfsTer?
|
|
XM_011520117.1:c.2824_2825del
|
XP_011518419.1:p.Asn942TyrfsTer?
|
|
XM_011520118.1:c.2761_2762del
|
XP_011518420.1:p.Asn921TyrfsTer?
|
|