|
NM_032119.4:c.16886G>A
MANE Select
|
NP_115495.3:p.Trp5629Ter
|
|
ENST00000405460.9:c.16886G>A
MANE Select
|
ENSP00000384582.2:p.Trp5629Ter
|
|
NM_032119.3:c.16886G>A
|
NP_115495.3:p.Trp5629Ter
|
|
NR_003149.1:n.16899G>A
|
|
|
NR_003149.2:n.16902G>A
|
|
|
ENST00000405460.6:c.16886G>A
|
ENSP00000384582.2:p.Trp5629Ter
|
|
ENST00000425867.2:c.3869G>A
|
ENSP00000392618.2:p.Trp1290Ter
|
|
ENST00000425867.3:c.5840G>A
|
ENSP00000392618.3:p.Trp1947Ter
|
|
ENST00000638510.1:n.4153G>A
|
|
|
ENST00000639431.1:c.266-144492G>A
|
ENSP00000491057.1:n.266-144492G>A
|
|
ENST00000640061.1:n.403G>A
|
|
|
ENST00000640407.1:c.3335G>A
|
ENSP00000491425.1:n.3335G>A
|
|
XM_011543675.1:c.16883G>A
|
XP_011541977.1:p.Trp5628Ter
|
|
XM_011543676.1:c.16805G>A
|
XP_011541978.1:p.Trp5602Ter
|
|
XM_011543677.1:c.14189G>A
|
XP_011541979.1:p.Trp4730Ter
|
|
XM_017009963.2:c.16907G>A
|
XP_016865452.1:p.Trp5636Ter
|
|
XM_017009964.2:c.16904G>A
|
XP_016865453.1:p.Trp5635Ter
|
|
XM_017009965.1:c.16904G>A
|
XP_016865454.1:p.Trp5635Ter
|
|
XM_017009966.2:c.16826G>A
|
XP_016865455.1:p.Trp5609Ter
|
|
XM_017009967.1:c.16811G>A
|
XP_016865456.1:p.Trp5604Ter
|
|
XM_017009968.2:c.16727G>A
|
XP_016865457.1:p.Trp5576Ter
|
|
XM_017009969.2:c.16907G>A
|
XP_016865458.1:p.Trp5636Ter
|
|
XM_017009972.1:c.10025G>A
|
XP_016865461.1:p.Trp3342Ter
|
|
XM_017009973.1:c.10004G>A
|
XP_016865462.1:p.Trp3335Ter
|