|
ENST00000356660.9:c.236C>A
(BDNF)
MANE Select
|
ENSP00000349084.4:p.Pro79His
|
|
|
ENST00000314915.6:c.260C>A
(BDNF)
|
ENSP00000320002.6:p.Pro87His
|
|
|
ENST00000356660.8:c.236C>A
(BDNF)
|
ENSP00000349084.4:p.Pro79His
|
|
|
ENST00000395978.7:c.236C>A
(BDNF)
|
ENSP00000379302.3:p.Pro79His
|
|
|
ENST00000395980.6:c.236C>A
(BDNF)
|
ENSP00000379304.2:p.Pro79His
|
|
|
ENST00000395981.7:c.236C>A
(BDNF)
|
ENSP00000379305.3:p.Pro79His
|
|
|
ENST00000395983.7:c.236C>A
(BDNF)
|
ENSP00000379307.3:p.Pro79His
|
|
|
ENST00000395986.6:c.281C>A
(BDNF)
|
ENSP00000379309.2:p.Pro94His
|
|
|
ENST00000418212.5:c.236C>A
(BDNF)
|
ENSP00000400502.1:p.Pro79His
|
|
|
ENST00000420794.2:c.236C>A
(BDNF)
|
ENSP00000389564.1:p.Pro79His
|
|
|
ENST00000438929.5:c.482C>A
(BDNF)
|
ENSP00000414303.1:p.Pro161His
|
|
|
ENST00000439476.6:c.236C>A
(BDNF)
|
ENSP00000389345.2:p.Pro79His
|
|
|
ENST00000525528.1:c.236C>A
(BDNF)
|
ENSP00000437138.1:p.Pro79His
|
|
|
ENST00000525950.5:c.236C>A
(BDNF)
|
ENSP00000432035.1:p.Pro79His
|
|
|
ENST00000530786.5:c.*365C>A
(BDNF)
|
ENSP00000433003.1:n.*365C>A
|
|
|
ENST00000530861.5:c.236C>A
(BDNF)
|
ENSP00000435564.1:p.Pro79His
|
|
|
ENST00000532997.5:c.236C>A
(BDNF)
|
ENSP00000435805.1:p.Pro79His
|
|
|
ENST00000533131.5:c.236C>A
(BDNF)
|
ENSP00000432727.1:p.Pro79His
|
|
|
ENST00000533246.5:c.236C>A
(BDNF)
|
ENSP00000432376.1:p.Pro79His
|
|
|
ENST00000584049.5:n.594C>A
(BDNF)
|
|
|
|
NM_001143805.1:c.236C>A
(BDNF)
|
NP_001137277.1:p.Pro79His
|
|
|
NM_001143806.1:c.236C>A
(BDNF)
|
NP_001137278.1:p.Pro79His
|
|
|
NM_001143807.1:c.236C>A
(BDNF)
|
NP_001137279.1:p.Pro79His
|
|
|
NM_001143808.1:c.236C>A
(BDNF)
|
NP_001137280.1:p.Pro79His
|
|
|
NM_001143809.1:c.323C>A
(BDNF)
|
NP_001137281.1:p.Pro108His
|
|
|
NM_001143810.1:c.482C>A
(BDNF)
|
NP_001137282.1:p.Pro161His
|
|
|
NM_001143811.1:c.236C>A
(BDNF)
|
NP_001137283.1:p.Pro79His
|
|
|
NM_001143812.1:c.236C>A
(BDNF)
|
NP_001137284.1:p.Pro79His
|
|
|
NM_001143813.1:c.236C>A
(BDNF)
|
NP_001137285.1:p.Pro79His
|
|
|
NM_001143814.1:c.236C>A
(BDNF)
|
NP_001137286.1:p.Pro79His
|
|
|
NM_001143816.1:c.236C>A
(BDNF)
|
NP_001137288.1:p.Pro79His
|
|
|
NM_001709.4:c.236C>A
(BDNF)
|
NP_001700.2:p.Pro79His
|
|
|
NM_170731.4:c.260C>A
(BDNF)
|
NP_733927.1:p.Pro87His
|
|
|
NM_170732.4:c.236C>A
(BDNF)
|
NP_733928.1:p.Pro79His
|
|
|
NM_170733.3:c.236C>A
(BDNF)
|
NP_733929.1:p.Pro79His
|
|
|
NM_170734.3:c.281C>A
(BDNF)
|
NP_733930.1:p.Pro94His
|
|
|
NM_170735.5:c.236C>A
(BDNF)
|
NP_733931.1:p.Pro79His
|
|
|
NR_002832.2:n.463G>T
(BDNF-AS)
|
|
|
|
NR_033312.1:n.394G>T
(BDNF-AS)
|
|
|
|
NR_033313.1:n.394G>T
(BDNF-AS)
|
|
|
|
NR_033314.1:n.463G>T
(BDNF-AS)
|
|
|
|
NR_033315.1:n.394G>T
(BDNF-AS)
|
|
|
|
XM_011520280.1:c.482C>A
(BDNF)
|
XP_011518582.1:p.Pro161His
|
|
|
XM_011520280.2:c.482C>A
(BDNF)
|
XP_011518582.1:p.Pro161His
|
|
|
NM_001709.5:c.236C>A
(BDNF)
MANE Select
|
NP_001700.2:p.Pro79His
|
|
|
NM_001143807.2:c.236C>A
(BDNF)
|
NP_001137279.1:p.Pro79His
|
|
|
NM_001143813.2:c.236C>A
(BDNF)
|
NP_001137285.1:p.Pro79His
|
|
|
NM_001143814.2:c.236C>A
(BDNF)
|
NP_001137286.1:p.Pro79His
|
|
|
NM_170731.5:c.260C>A
(BDNF)
|
NP_733927.1:p.Pro87His
|
|
|
NM_001143808.2:c.236C>A
(BDNF)
|
NP_001137280.1:p.Pro79His
|
|
|
NM_001143809.2:c.323C>A
(BDNF)
|
NP_001137281.1:p.Pro108His
|
|
|
NM_001143810.2:c.482C>A
(BDNF)
|
NP_001137282.1:p.Pro161His
|
|
|
NM_001143811.2:c.236C>A
(BDNF)
|
NP_001137283.1:p.Pro79His
|
|
|
NM_001143812.2:c.236C>A
(BDNF)
|
NP_001137284.1:p.Pro79His
|
|
|
NM_001143816.2:c.236C>A
(BDNF)
|
NP_001137288.1:p.Pro79His
|
|
|
NM_170733.4:c.236C>A
(BDNF)
|
NP_733929.1:p.Pro79His
|
|
|
NM_170734.4:c.281C>A
(BDNF)
|
NP_733930.1:p.Pro94His
|
|
|
NM_170735.6:c.236C>A
(BDNF)
|
NP_733931.1:p.Pro79His
|
|
