ENST00000405460.9:c.9383A>T
MANE Select
|
ENSP00000384582.2:p.Asn3128Ile
|
|
ENST00000639431.1:c.265+40456A>T
|
ENSP00000491057.1:n.265+40456A>T
|
|
ENST00000639473.1:n.4842A>T
|
|
|
ENST00000640012.1:c.3190A>T
|
|
|
ENST00000640374.1:n.2527A>T
|
|
|
ENST00000640779.1:c.4112A>T
|
|
|
ENST00000405460.6:c.9383A>T
|
ENSP00000384582.2:p.Asn3128Ile
|
|
ENST00000509621.1:c.2080A>T
|
|
|
NM_032119.3:c.9383A>T
|
NP_115495.3:p.Asn3128Ile
|
|
NR_003149.1:n.9396A>T
|
|
|
XM_011543675.1:c.9380A>T
|
XP_011541977.1:p.Asn3127Ile
|
|
XM_011543676.1:c.9302A>T
|
XP_011541978.1:p.Asn3101Ile
|
|
XM_011543677.1:c.6686A>T
|
XP_011541979.1:p.Asn2229Ile
|
|
XM_011543678.1:c.9383A>T
|
XP_011541980.1:p.Asn3128Ile
|
|
XM_011543679.1:c.9383A>T
|
XP_011541981.1:p.Asn3128Ile
|
|
XR_948560.1:n.272-856T>A
|
|
|
NM_032119.4:c.9383A>T
MANE Select
|
NP_115495.3:p.Asn3128Ile
|
|
XM_017009963.2:c.9404A>T
|
XP_016865452.1:p.Asn3135Ile
|
|
XM_017009964.2:c.9401A>T
|
XP_016865453.1:p.Asn3134Ile
|
|
XM_017009965.1:c.9401A>T
|
XP_016865454.1:p.Asn3134Ile
|
|
XM_017009966.2:c.9323A>T
|
XP_016865455.1:p.Asn3108Ile
|
|
XM_017009967.1:c.9308A>T
|
XP_016865456.1:p.Asn3103Ile
|
|
XM_017009968.2:c.9404A>T
|
XP_016865457.1:p.Asn3135Ile
|
|
XM_017009969.2:c.9404A>T
|
XP_016865458.1:p.Asn3135Ile
|
|
XM_017009970.2:c.9404A>T
|
XP_016865459.1:p.Asn3135Ile
|
|
XM_017009971.2:c.9404A>T
|
XP_016865460.1:p.Asn3135Ile
|
|
XM_017009972.1:c.2522A>T
|
XP_016865461.1:p.Asn841Ile
|
|
XM_017009973.1:c.2501A>T
|
XP_016865462.1:p.Asn834Ile
|
|
XM_017009974.2:c.9404A>T
|
XP_016865463.1:p.Asn3135Ile
|
|
XR_001742802.1:n.2523-856T>A
|
|
|
NR_003149.2:n.9399A>T
|
|
|