ENST00000449606.7:c.798G>A
MANE Select
|
ENSP00000395196.2:p.Trp266Ter
|
|
ENST00000674054.1:c.798G>A
|
ENSP00000501251.1:p.Trp266Ter
|
|
ENST00000449606.5:c.798G>A
|
ENSP00000395196.1:p.Trp266Ter
|
|
ENST00000562402.1:n.402G>A
|
|
|
ENST00000563232.1:c.798G>A
|
ENSP00000456218.1:p.Trp266Ter
|
|
ENST00000563459.5:c.798G>A
|
ENSP00000456467.1:p.Trp266Ter
|
|
ENST00000564501.5:c.798G>A
|
ENSP00000457107.1:p.Trp266Ter
|
|
ENST00000564987.1:n.422G>A
|
|
|
ENST00000565344.1:n.171G>A
|
|
|
NM_001083614.1:c.798G>A
|
NP_001077083.1:p.Trp266Ter
|
|
NM_001308211.1:c.798G>A
|
NP_001295140.1:p.Trp266Ter
|
|
NR_003501.1:n.830G>A
|
|
|
XM_011545738.1:c.726G>A
|
XP_011544040.1:p.Trp242Ter
|
|
XM_011545739.1:c.519G>A
|
XP_011544041.1:p.Trp173Ter
|
|
XR_001751841.1:n.1120G>A
|
|
|
NM_001083614.2:c.798G>A
MANE Select
|
NP_001077083.1:p.Trp266Ter
|
|
NR_003501.2:n.805G>A
|
|
|