ENST00000405460.9:c.14281C>A
MANE Select
|
ENSP00000384582.2:p.His4761Asn
|
|
ENST00000425867.3:c.3235C>A
|
ENSP00000392618.3:p.His1079Asn
|
|
ENST00000638510.1:n.1548C>A
|
|
|
ENST00000638585.1:n.47C>A
|
|
|
ENST00000638975.1:c.910C>A
|
ENSP00000492630.1:p.His304Asn
|
|
ENST00000639431.1:c.265+114901C>A
|
ENSP00000491057.1:n.265+114901C>A
|
|
ENST00000640407.1:c.691C>A
|
ENSP00000491425.1:p.His231Asn
|
|
ENST00000405460.6:c.14281C>A
|
ENSP00000384582.2:p.His4761Asn
|
|
ENST00000425867.2:c.1264C>A
|
ENSP00000392618.2:p.His422Asn
|
|
NM_032119.3:c.14281C>A
|
NP_115495.3:p.His4761Asn
|
|
NR_003149.1:n.14294C>A
|
|
|
XM_011543675.1:c.14278C>A
|
XP_011541977.1:p.His4760Asn
|
|
XM_011543676.1:c.14200C>A
|
XP_011541978.1:p.His4734Asn
|
|
XM_011543677.1:c.11584C>A
|
XP_011541979.1:p.His3862Asn
|
|
XM_011543678.1:c.14281C>A
|
XP_011541980.1:p.His4761Asn
|
|
NM_032119.4:c.14281C>A
MANE Select
|
NP_115495.3:p.His4761Asn
|
|
XM_017009963.2:c.14302C>A
|
XP_016865452.1:p.His4768Asn
|
|
XM_017009964.2:c.14299C>A
|
XP_016865453.1:p.His4767Asn
|
|
XM_017009965.1:c.14299C>A
|
XP_016865454.1:p.His4767Asn
|
|
XM_017009966.2:c.14221C>A
|
XP_016865455.1:p.His4741Asn
|
|
XM_017009967.1:c.14206C>A
|
XP_016865456.1:p.His4736Asn
|
|
XM_017009968.2:c.14302C>A
|
XP_016865457.1:p.His4768Asn
|
|
XM_017009969.2:c.14302C>A
|
XP_016865458.1:p.His4768Asn
|
|
XM_017009970.2:c.14302C>A
|
XP_016865459.1:p.His4768Asn
|
|
XM_017009971.2:c.14302C>A
|
XP_016865460.1:p.His4768Asn
|
|
XM_017009972.1:c.7420C>A
|
XP_016865461.1:p.His2474Asn
|
|
XM_017009973.1:c.7399C>A
|
XP_016865462.1:p.His2467Asn
|
|
NR_003149.2:n.14297C>A
|
|
|