|
Q5QTR7
|
APID
|
UniProt
|
GRPSRTSSSGSSSS
|
68-81
|
22.56
|
nd
|
nd
|
nd
|
nd
|
Q5QTR7_HUMAN FWP009 - Homo sapiens
|
|
Q8WXS5
|
APID
|
UniProt
|
AERDRGGSSGFLTL
|
355-368
|
22.56
|
nd
|
nd
|
nd
|
nd
|
CCG8_HUMAN Voltage-dependent calcium channel gamma-8 subunit - Homo sapiens
|
|
A8K064
|
APID
|
UniProt
|
SNFRGGSDGYGSGR
|
225-238
|
22.56
|
nd
|
nd
|
nd
|
nd
|
A8K064_HUMAN cDNA FLJ75945, highly similar to Homo sapiens heterogeneous nuclear ribonucleoprotein A2/B1 (HNRPA2B1), transcript variant B1, mRNA - Homo sapiens
|
|
Q5THK1
|
APID
|
UniProt
|
SPHCKRQPSLGTTS
|
1905-1918
|
22.57
|
nd
|
nd
|
nd
|
nd
|
CV030_HUMAN Uncharacterized protein C22orf30 - Homo sapiens
|
|
Q5BQ95
|
APID
|
UniProt
|
PHCRTLSKGGAQSL
|
73-86
|
22.57
|
nd
|
nd
|
nd
|
nd
|
Q5BQ95_HUMAN Kallikrein 13 splice variant 8 - Homo sapiens
|
|
O95678
|
APID
|
UniProt
|
LSSGYGRGSSIGGG
|
479-492
|
22.57
|
nd
|
nd
|
nd
|
nd
|
K2C75_HUMAN Keratin, type II cytoskeletal 75 - Homo sapiens
|
|
Q19QZ9
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19QZ9_HUMAN T calcium channel alpha 1G subunit variant 217 - Homo sapiens
|
|
Q19R17
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1040-1053
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19R17_HUMAN T calcium channel alpha 1G subunit variant 25 - Homo sapiens
|
|
Q19R13
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1040-1053
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19R13_HUMAN T calcium channel alpha 1G subunit variant 88 - Homo sapiens
|
|
Q19R05
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19R05_HUMAN T calcium channel alpha 1G subunit variant 177 - Homo sapiens
|
|
Q19QY9
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19QY9_HUMAN T calcium channel alpha 1G subunit variant 473-d81 - Homo sapiens
|
|
Q19R10
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19R10_HUMAN T calcium channel alpha 1G subunit variant 137 - Homo sapiens
|
|
Q19QZ7
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19QZ7_HUMAN T calcium channel alpha 1G subunit variant 223 - Homo sapiens
|
|
Q19QZ4
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19QZ4_HUMAN T calcium channel alpha 1G subunit variant 409 - Homo sapiens
|
|
Q19R02
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19R02_HUMAN T calcium channel alpha 1G subunit variant 189 - Homo sapiens
|
|
Q19QZ3
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19QZ3_HUMAN T calcium channel alpha 1G subunit variant 441 - Homo sapiens
|
|
Q19R08
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19R08_HUMAN T calcium channel alpha 1G subunit variant 153 - Homo sapiens
|
|
Q19QZ6
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19QZ6_HUMAN T calcium channel alpha 1G subunit variant 249 - Homo sapiens
|
|
Q19R00
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1063-1076
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19R00_HUMAN T calcium channel alpha 1G subunit variant 216 - Homo sapiens
|
|
Q19R16
|
APID
|
UniProt
|
GPASRRTSSSGSAE
|
1040-1053
|
22.58
|
nd
|
nd
|
nd
|
nd
|
Q19R16_HUMAN T calcium channel alpha 1G subunit variant 33 - Homo sapiens
|