ENST00000576892.8:c.512G>A
MANE Select
|
ENSP00000461135.1:p.Trp171Ter
|
|
ENST00000429336.5:c.193+1896G>A
|
|
|
ENST00000440428.5:c.512G>A
|
ENSP00000402949.2:p.Trp171Ter
|
|
ENST00000482182.3:c.386G>A
|
ENSP00000466345.1:p.Trp129Ter
|
|
ENST00000576892.7:c.512G>A
|
ENSP00000461135.1:p.Trp171Ter
|
|
ENST00000614850.1:c.277+3353G>A
|
|
|
ENST00000614851.4:c.333G>A
|
|
|
ENST00000620088.4:c.*388G>A
|
ENSP00000484108.1:n.*388G>A
|
|
ENST00000621629.4:c.*388G>A
|
ENSP00000478747.1:n.*388G>A
|
|
ENST00000621817.1:c.*677G>A
|
ENSP00000481634.1:n.*677G>A
|
|
NM_001130997.2:c.512G>A
|
NP_001124469.1:p.Trp171Ter
|
|
NM_152274.4:c.512G>A
|
NP_689487.2:p.Trp171Ter
|
|
XM_005277920.3:c.482G>A
|
XP_005277977.1:p.Trp161Ter
|
|
XM_005277921.3:c.482G>A
|
XP_005277978.1:p.Trp161Ter
|
|
XM_011531213.1:c.386G>A
|
XP_011529515.1:p.Trp129Ter
|
|
XM_011531214.1:c.386G>A
|
XP_011529516.1:p.Trp129Ter
|
|
XM_011531215.1:c.386G>A
|
XP_011529517.1:p.Trp129Ter
|
|
XM_005277920.4:c.482G>A
|
XP_005277977.1:p.Trp161Ter
|
|
XM_005277921.4:c.482G>A
|
XP_005277978.1:p.Trp161Ter
|
|
XM_011531214.2:c.386G>A
|
XP_011529516.1:p.Trp129Ter
|
|
XM_011531215.2:c.386G>A
|
XP_011529517.1:p.Trp129Ter
|
|
XR_002958810.1:n.2417G>A
|
|
|
NM_152274.5:c.512G>A
MANE Select
|
NP_689487.2:p.Trp171Ter
|
|
NM_001130997.3:c.512G>A
|
NP_001124469.1:p.Trp171Ter
|
|