|
Q9UDY2
|
APID
|
UniProt
|
RLNSHG
|
160-165
|
7.41
|
MINT-50823
|
1
|
0.19
|
15324660
|
ZO2_HUMAN Tight junction protein ZO-2 - Homo sapiens
|
|
Q19R05
|
APID
|
UniProt
|
RQRSLG
|
712-717
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q19R05_HUMAN T calcium channel alpha 1G subunit variant 177 - Homo sapiens
|
|
Q5VW27
|
APID
|
UniProt
|
RSLSSP
|
261-266
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q5VW27_HUMAN Nuclear factor 1 - Homo sapiens
|
|
Q19R17
|
APID
|
UniProt
|
RQRSLG
|
712-717
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q19R17_HUMAN T calcium channel alpha 1G subunit variant 25 - Homo sapiens
|
|
Q63HM5
|
APID
|
UniProt
|
RSLSSP
|
9-14
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q63HM5_HUMAN Putative uncharacterized protein DKFZp686E13259 - Homo sapiens
|
|
Q13029
|
APID
|
UniProt
|
RARSSG
|
1535-1540
|
7.41
|
nd
|
nd
|
nd
|
nd
|
PRDM2_HUMAN PR domain zinc finger protein 2 - Homo sapiens
|
|
Q19QZ0
|
APID
|
UniProt
|
RQRSLG
|
712-717
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q19QZ0_HUMAN T calcium channel alpha 1G subunit variant 473-d75 - Homo sapiens
|
|
Q19R00
|
APID
|
UniProt
|
RQRSLG
|
712-717
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q19R00_HUMAN T calcium channel alpha 1G subunit variant 216 - Homo sapiens
|
|
Q8N2U6
|
APID
|
UniProt
|
RQRSLG
|
180-185
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q8N2U6_HUMAN CCDC88B protein - Homo sapiens
|
|
Q19QZ3
|
APID
|
UniProt
|
RQRSLG
|
712-717
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q19QZ3_HUMAN T calcium channel alpha 1G subunit variant 441 - Homo sapiens
|
|
A2A3H9
|
APID
|
UniProt
|
RLNSHG
|
160-165
|
7.41
|
nd
|
nd
|
nd
|
nd
|
A2A3H9_HUMAN Tight junction protein 2 - Homo sapiens
|
|
Q19QZ1
|
APID
|
UniProt
|
RQRSLG
|
712-717
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q19QZ1_HUMAN T calcium channel alpha 1G subunit variant 473 - Homo sapiens
|
|
Q6ZNF9
|
APID
|
UniProt
|
RSLSSP
|
287-292
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q6ZNF9_HUMAN cDNA FLJ16142 fis, clone BRAMY2035718, highly similar to NUCLEAR FACTOR 1-B - Homo sapiens
|
|
O00712
|
APID
|
UniProt
|
RSLSSP
|
261-266
|
7.41
|
nd
|
nd
|
nd
|
nd
|
NFIB_HUMAN Nuclear factor 1 B-type - Homo sapiens
|
|
Q19QY8
|
APID
|
UniProt
|
RQRSLG
|
712-717
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q19QY8_HUMAN T calcium channel alpha 1G subunit variant 477 - Homo sapiens
|
|
Q19QZ5
|
APID
|
UniProt
|
RQRSLG
|
712-717
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q19QZ5_HUMAN T calcium channel alpha 1G subunit variant 313 - Homo sapiens
|
|
Q19R08
|
APID
|
UniProt
|
RQRSLG
|
712-717
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q19R08_HUMAN T calcium channel alpha 1G subunit variant 153 - Homo sapiens
|
|
Q19R13
|
APID
|
UniProt
|
RQRSLG
|
712-717
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q19R13_HUMAN T calcium channel alpha 1G subunit variant 88 - Homo sapiens
|
|
Q19QZ7
|
APID
|
UniProt
|
RQRSLG
|
712-717
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q19QZ7_HUMAN T calcium channel alpha 1G subunit variant 223 - Homo sapiens
|
|
Q19QZ6
|
APID
|
UniProt
|
RQRSLG
|
712-717
|
7.41
|
nd
|
nd
|
nd
|
nd
|
Q19QZ6_HUMAN T calcium channel alpha 1G subunit variant 249 - Homo sapiens
|