|
A8MUW2
|
APID
|
UniProt
|
PKHAHRHPDTPTPRHTFT
|
219-236
|
7.35
|
nd
|
nd
|
nd
|
nd
|
A8MUW2_HUMAN Uncharacterized protein ENSP00000382634 - Homo sapiens
|
|
Q8TES7
|
APID
|
UniProt
|
QSPPMASSPIQPRKGGAD
|
327-344
|
7.35
|
nd
|
nd
|
nd
|
nd
|
FBF1_HUMAN Fas-binding factor 1 - Homo sapiens
|
|
Q8IXK1
|
APID
|
UniProt
|
TRGPEGTPKATPTTSRPS
|
503-520
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q8IXK1_HUMAN C1q receptor protein precursor - Homo sapiens
|
|
Q6NSK3
|
APID
|
UniProt
|
FSQPERPFLAPGRQSVDN
|
976-993
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q6NSK3_HUMAN RBM16 protein - Homo sapiens
|
|
Q92922
|
APID
|
UniProt
|
KHSPSPPPPTPTESRKKS
|
326-343
|
7.35
|
nd
|
nd
|
nd
|
nd
|
SMRC1_HUMAN SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily C member 1 - Homo sapiens
|
|
Q5T6W5
|
APID
|
UniProt
|
LPLPPPPPPRGGDLMAYD
|
272-289
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q5T6W5_HUMAN Heterogeneous nuclear ribonucleoprotein K - Homo sapiens
|
|
Q58EY4
|
APID
|
UniProt
|
KHSPSPPPPTPTESRKKS
|
326-343
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q58EY4_HUMAN SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 1 - Homo sapiens
|
|
Q19R15
|
APID
|
UniProt
|
QAPPPRSPSEASGRTVGS
|
569-586
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q19R15_HUMAN T calcium channel alpha 1G subunit variant 49 - Homo sapiens
|
|
Q5H9S4
|
APID
|
UniProt
|
PPMGFTTPPLDPVLQNPL
|
494-511
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q5H9S4_HUMAN Putative uncharacterized protein DKFZp686A01127 - Homo sapiens
|
|
Q5EC54
|
APID
|
UniProt
|
LPLPPPPPPRGGDLMAYD
|
307-324
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q5EC54_HUMAN Heterogeneous nuclear ribonucleoprotein K transcript variant - Homo sapiens
|
|
Q15562
|
APID
|
UniProt
|
SGPPWNVPDVKPFSQTPF
|
168-185
|
7.35
|
nd
|
nd
|
nd
|
nd
|
TEAD2_HUMAN Transcriptional enhancer factor TEF-4 - Homo sapiens
|
|
Q19R03
|
APID
|
UniProt
|
QAPPPRSPSEASGRTVGS
|
569-586
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q19R03_HUMAN T calcium channel alpha 1G subunit variant 185 - Homo sapiens
|
|
Q19QZ9
|
APID
|
UniProt
|
QAPPPRSPSEASGRTVGS
|
569-586
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q19QZ9_HUMAN T calcium channel alpha 1G subunit variant 217 - Homo sapiens
|
|
Q19R09
|
APID
|
UniProt
|
QAPPPRSPSEASGRTVGS
|
569-586
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q19R09_HUMAN T calcium channel alpha 1G subunit variant 145 - Homo sapiens
|
|
Q6IBN1
|
APID
|
UniProt
|
LPLPPPPPPRGGDLMAYD
|
307-324
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q6IBN1_HUMAN HNRPK protein - Homo sapiens
|
|
O94761
|
APID
|
UniProt
|
PEVPSLDPTVLPLYSLGP
|
441-458
|
7.35
|
nd
|
nd
|
nd
|
nd
|
RECQ4_HUMAN ATP-dependent DNA helicase Q4 - Homo sapiens
|
|
Q19R08
|
APID
|
UniProt
|
QAPPPRSPSEASGRTVGS
|
569-586
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q19R08_HUMAN T calcium channel alpha 1G subunit variant 153 - Homo sapiens
|
|
Q5SZP3
|
APID
|
UniProt
|
MSKPGRKLAEVPPCVQPT
|
351-368
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q5SZP3_HUMAN Paired box gene 2 - Homo sapiens
|
|
Q1JQ81
|
APID
|
UniProt
|
NIPPHGVPMGPGLMSHNP
|
1101-1118
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q1JQ81_HUMAN B-cell CLL/lymphoma 9 - Homo sapiens
|
|
Q19QZ1
|
APID
|
UniProt
|
QAPPPRSPSEASGRTVGS
|
569-586
|
7.35
|
nd
|
nd
|
nd
|
nd
|
Q19QZ1_HUMAN T calcium channel alpha 1G subunit variant 473 - Homo sapiens
|