|
ENST00000405460.9:c.16245_16248delinsAGTC
MANE Select
|
ENSP00000384582.2:p.Thr5415=
|
|
|
ENST00000425867.3:c.5199_5202delinsAGTC
|
ENSP00000392618.3:p.Thr1733=
|
|
|
ENST00000638510.1:n.3512_3515delinsAGTC
|
|
|
|
ENST00000639431.1:c.265+147264_265+147267delinsAGTC
|
ENSP00000491057.1:n.265+147264_265+147267...
|
|
|
ENST00000640061.1:n.128+1291_128+1294delinsAGTC
|
|
|
|
ENST00000640407.1:c.2655_2658delinsAGTC
|
ENSP00000491425.1:p.Thr885=
|
|
|
ENST00000405460.6:c.16245_16248delinsAGTC
|
ENSP00000384582.2:p.Thr5415=
|
|
|
ENST00000425867.2:c.3228_3231delinsAGTC
|
ENSP00000392618.2:p.Thr1076=
|
|
|
NM_032119.3:c.16245_16248delinsAGTC
|
NP_115495.3:p.Thr5415=
|
|
|
NR_003149.1:n.16258_16261delinsAGTC
|
|
|
|
XM_011543675.1:c.16242_16245delinsAGTC
|
XP_011541977.1:p.Thr5414=
|
|
|
XM_011543676.1:c.16164_16167delinsAGTC
|
XP_011541978.1:p.Thr5388=
|
|
|
XM_011543677.1:c.13548_13551delinsAGTC
|
XP_011541979.1:p.Thr4516=
|
|
|
NM_032119.4:c.16245_16248delinsAGTC
MANE Select
|
NP_115495.3:p.Thr5415=
|
|
|
XM_017009963.2:c.16266_16269delinsAGTC
|
XP_016865452.1:p.Thr5422=
|
|
|
XM_017009964.2:c.16263_16266delinsAGTC
|
XP_016865453.1:p.Thr5421=
|
|
|
XM_017009965.1:c.16263_16266delinsAGTC
|
XP_016865454.1:p.Thr5421=
|
|
|
XM_017009966.2:c.16185_16188delinsAGTC
|
XP_016865455.1:p.Thr5395=
|
|
|
XM_017009967.1:c.16170_16173delinsAGTC
|
XP_016865456.1:p.Thr5390=
|
|
|
XM_017009968.2:c.16086_16089delinsAGTC
|
XP_016865457.1:p.Thr5362=
|
|
|
XM_017009969.2:c.16266_16269delinsAGTC
|
XP_016865458.1:p.Thr5422=
|
|
|
XM_017009972.1:c.9384_9387delinsAGTC
|
XP_016865461.1:p.Thr3128=
|
|
|
XM_017009973.1:c.9363_9366delinsAGTC
|
XP_016865462.1:p.Thr3121=
|
|
|
NR_003149.2:n.16261_16264delinsAGTC
|
|
|
