|
ENST00000713589.1:c.830G>A
(C1QTNF9B)
MANE Select
|
ENSP00000518885.1:p.Arg277Lys
|
|
NM_001007537.2:c.830G>A
(C1QTNF9B)
|
NP_001007538.1:p.Arg277Lys
|
|
NM_001014442.2:c.-66C>T
(PCOTH)
|
NP_001014442.2:n.-66C>T
|
|
NM_001014442.3:c.-66C>T
(PCOTH)
|
NP_001014442.2:n.-66C>T
|
|
NM_001014442.4:c.-66C>T
(PCOTH)
|
NP_001014442.2:n.-66C>T
|
|
NM_001135816.1:c.32+11C>T
(PCOTH)
|
NP_001129288.1:n.32+11C>T
|
|
NM_001135816.2:c.32+11C>T
(PCOTH)
|
NP_001129288.1:n.32+11C>T
|
|
NM_001135816.3:c.32+11C>T
(PCOTH)
|
NP_001129288.1:n.32+11C>T
|
|
NM_001348112.1:c.32+11C>T
(PCOTH)
|
NP_001335041.1:n.32+11C>T
|
|
NM_001348112.2:c.32+11C>T
(PCOTH)
|
NP_001335041.1:n.32+11C>T
|
|
NM_001348113.1:c.-66C>T
(PCOTH)
|
NP_001335042.1:n.-66C>T
|
|
NM_001348113.2:c.-66C>T
(PCOTH)
|
NP_001335042.1:n.-66C>T
|
|
NM_001348114.1:c.-66C>T
(PCOTH)
|
NP_001335043.1:n.-66C>T
|
|
NM_001348114.2:c.-66C>T
(PCOTH)
|
NP_001335043.1:n.-66C>T
|
|
NR_104426.1:n.526G>A
(C1QTNF9B)
|
|
|
NR_172510.1:n.264C>T
(PCOTH)
|
|
|
NR_172511.1:n.197+11C>T
(PCOTH)
|
|
|
NR_172512.1:n.312+11C>T
(PCOTH)
|
|
|
NR_172513.1:n.208C>T
(PCOTH)
|
|
|
NR_172514.1:n.322C>T
(PCOTH)
|
|
|
NR_172515.1:n.381+11C>T
(PCOTH)
|
|
|
NR_172516.1:n.392C>T
(PCOTH)
|
|
|
ENST00000382137.7:c.830G>A
(C1QTNF9B)
|
ENSP00000371572.3:p.Arg277Lys
|
|
ENST00000382137.8:c.830G>A
(C1QTNF9B)
|
ENSP00000371572.3:p.Arg277Lys
|
|
ENST00000382140.2:c.830G>A
(C1QTNF9B)
|
ENSP00000371575.2:p.Arg277Lys
|
|
ENST00000382145.5:c.*16G>A
(C1QTNF9B)
|
ENSP00000371580.1:n.*16G>A
|
|
ENST00000556521.1:n.517G>A
(C1QTNF9B)
|
|
|
XM_011535070.1:c.830G>A
(C1QTNF9B)
|
XP_011533372.1:p.Arg277Lys
|
