ENST00000234071.8:c.560G>A
MANE Select
|
ENSP00000234071.4:p.Trp187Ter
|
|
ENST00000234071.7:c.560G>A
|
ENSP00000234071.3:p.Trp187Ter
|
|
ENST00000402125.2:c.121-2248G>A
|
|
|
ENST00000409048.1:c.662G>A
|
ENSP00000386679.1:p.Trp221Ter
|
|
ENST00000442644.5:c.503G>A
|
ENSP00000411241.1:p.Trp168Ter
|
|
ENST00000464089.1:n.146G>A
|
|
|
NM_000312.3:c.560G>A , LRG_599t1:c.560G>A
|
NP_000303.1:p.Trp187Ter
|
|
XM_005263715.3:c.743G>A
|
XP_005263772.1:p.Trp248Ter
|
|
XM_005263716.3:c.725G>A
|
XP_005263773.1:p.Trp242Ter
|
|
XM_005263717.3:c.623G>A
|
XP_005263774.1:p.Trp208Ter
|
|
XM_005263717.4:c.623G>A
|
XP_005263774.1:p.Trp208Ter
|
|
XM_017004505.1:c.803G>A
|
XP_016859994.1:p.Trp268Ter
|
|
XM_024453002.1:c.905G>A
|
XP_024308770.1:p.Trp302Ter
|
|
XM_024453003.1:c.845G>A
|
XP_024308771.1:p.Trp282Ter
|
|
XM_024453004.1:c.743G>A
|
XP_024308772.1:p.Trp248Ter
|
|
XM_024453005.1:c.725G>A
|
XP_024308773.1:p.Trp242Ter
|
|
XM_024453006.1:c.662G>A
|
XP_024308774.1:p.Trp221Ter
|
|
XR_923313.2:n.4476C>T
|
|
|
NM_000312.4:c.560G>A
MANE Select
|
NP_000303.1:p.Trp187Ter
|
|
NM_001375602.1:c.743G>A
|
NP_001362531.1:p.Trp248Ter
|
|
NM_001375603.1:c.725G>A
|
NP_001362532.1:p.Trp242Ter
|
|
NM_001375604.1:c.623G>A
|
NP_001362533.1:p.Trp208Ter
|
|
NM_001375605.1:c.662G>A
|
NP_001362534.1:p.Trp221Ter
|
|
NM_001375606.1:c.728G>A
|
NP_001362535.1:p.Trp243Ter
|
|
NM_001375607.1:c.746G>A
|
NP_001362536.1:p.Trp249Ter
|
|
NM_001375608.1:c.503G>A
|
NP_001362537.1:p.Trp168Ter
|
|
NM_001375609.1:c.536G>A
|
NP_001362538.1:p.Trp179Ter
|
|
NM_001375610.1:c.554G>A
|
NP_001362539.1:p.Trp185Ter
|
|
NM_001375611.1:c.560G>A
|
NP_001362540.1:p.Trp187Ter
|
|
NM_001375613.1:c.560G>A
|
NP_001362542.1:p.Trp187Ter
|
|