|
ENST00000234071.8:c.561_562delinsGA
MANE Select
|
ENSP00000234071.4:p.Trp187=
|
|
|
ENST00000234071.7:c.561_562delinsGA
|
ENSP00000234071.3:p.Trp187=
|
|
|
ENST00000402125.2:c.121-2247_121-2246delinsGA
|
|
|
|
ENST00000409048.1:c.663_664delinsGA
|
ENSP00000386679.1:p.Trp221=
|
|
|
ENST00000442644.5:c.504_505delinsGA
|
ENSP00000411241.1:p.Trp168=
|
|
|
ENST00000464089.1:n.147_148delinsGA
|
|
|
|
NM_000312.3:c.561_562delinsGA , LRG_599t1:c.561_562delinsGA
|
NP_000303.1:p.Trp187=
|
|
|
XM_005263715.3:c.744_745delinsGA
|
XP_005263772.1:p.Trp248=
|
|
|
XM_005263716.3:c.726_727delinsGA
|
XP_005263773.1:p.Trp242=
|
|
|
XM_005263717.3:c.624_625delinsGA
|
XP_005263774.1:p.Trp208=
|
|
|
XM_005263717.4:c.624_625delinsGA
|
XP_005263774.1:p.Trp208=
|
|
|
XM_017004505.1:c.804_805delinsGA
|
XP_016859994.1:p.Trp268=
|
|
|
XM_024453002.1:c.906_907delinsGA
|
XP_024308770.1:p.Trp302=
|
|
|
XM_024453003.1:c.846_847delinsGA
|
XP_024308771.1:p.Trp282=
|
|
|
XM_024453004.1:c.744_745delinsGA
|
XP_024308772.1:p.Trp248=
|
|
|
XM_024453005.1:c.726_727delinsGA
|
XP_024308773.1:p.Trp242=
|
|
|
XM_024453006.1:c.663_664delinsGA
|
XP_024308774.1:p.Trp221=
|
|
|
XR_923313.2:n.4474_4475delinsTC
|
|
|
|
NM_000312.4:c.561_562delinsGA
MANE Select
|
NP_000303.1:p.Trp187=
|
|
|
NM_001375602.1:c.744_745delinsGA
|
NP_001362531.1:p.Trp248=
|
|
|
NM_001375603.1:c.726_727delinsGA
|
NP_001362532.1:p.Trp242=
|
|
|
NM_001375604.1:c.624_625delinsGA
|
NP_001362533.1:p.Trp208=
|
|
|
NM_001375605.1:c.663_664delinsGA
|
NP_001362534.1:p.Trp221=
|
|
|
NM_001375606.1:c.729_730delinsGA
|
NP_001362535.1:p.Trp243=
|
|
|
NM_001375607.1:c.747_748delinsGA
|
NP_001362536.1:p.Trp249=
|
|
|
NM_001375608.1:c.504_505delinsGA
|
NP_001362537.1:p.Trp168=
|
|
|
NM_001375609.1:c.537_538delinsGA
|
NP_001362538.1:p.Trp179=
|
|
|
NM_001375610.1:c.555_556delinsGA
|
NP_001362539.1:p.Trp185=
|
|
|
NM_001375611.1:c.561_562delinsGA
|
NP_001362540.1:p.Trp187=
|
|
|
NM_001375613.1:c.561_562delinsGA
|
NP_001362542.1:p.Trp187=
|
|
