ENST00000561514.3:c.3132_3133delinsTG
|
ENSP00000460666.3:p.Thr1044=
|
|
ENST00000565038.2:c.*607_*608delinsTG
|
ENSP00000459882.2:n.*607_*608delinsTG
|
|
ENST00000566069.6:c.3126_3127delinsTG
|
ENSP00000459237.2:p.Thr1042=
|
|
ENST00000697377.2:c.2970_2971delinsTG
|
ENSP00000513286.2:p.Thr990=
|
|
ENST00000697379.2:c.3132_3133delinsTG
|
ENSP00000513287.2:p.Thr1044=
|
|
ENST00000561514.2:c.2241_2242delinsTG
|
ENSP00000460666.2:p.Thr747=
|
|
ENST00000697374.1:c.2241_2242delinsTG
|
ENSP00000513284.1:p.Thr747=
|
|
ENST00000697375.1:n.4473_4474delinsTG
|
|
|
ENST00000697376.1:c.2241_2242delinsTG
|
ENSP00000513285.1:p.Thr747=
|
|
ENST00000697377.1:c.2079_2080delinsTG
|
ENSP00000513286.1:p.Thr693=
|
|
ENST00000697378.1:n.3646_3647delinsTG
|
|
|
ENST00000697379.1:c.2241_2242delinsTG
|
ENSP00000513287.1:p.Thr747=
|
|
ENST00000697380.1:n.2406-6067_2406-6066delinsTG
|
|
|
ENST00000697381.1:n.1821_1822delinsTG
|
|
|
ENST00000697382.1:c.2229-6067_2229-6066delinsTG
|
ENSP00000513288.1:n.2229-6067_2229-6066delinsTG
|
|
ENST00000697383.1:c.660_661delinsTG
|
ENSP00000513289.1:p.Thr220=
|
|
ENST00000261584.9:c.3126_3127delinsTG
MANE Select
|
ENSP00000261584.4:p.Thr1042=
|
|
ENST00000261584.8:c.3126_3127delinsTG
|
ENSP00000261584.4:p.Thr1042=
|
|
ENST00000566069.5:c.41_42delinsTG
|
|
|
ENST00000568219.5:c.2241_2242delinsTG
|
ENSP00000454703.2:p.Thr747=
|
|
NM_024675.3:c.3126_3127delinsTG , LRG_308t1:c.3126_3127delinsTG
|
NP_078951.2:p.Thr1042=
|
|
XM_011545946.1:c.3132_3133delinsTG
|
XP_011544248.1:p.Thr1044=
|
|
XM_011545947.1:c.3132_3133delinsTG
|
XP_011544249.1:p.Thr1044=
|
|
XM_011545948.1:c.2241_2242delinsTG
|
XP_011544250.1:p.Thr747=
|
|
XR_950851.1:n.3910-6067_3910-6066delinsTG
|
|
|
XM_011545946.2:c.3132_3133delinsTG
|
XP_011544248.1:p.Thr1044=
|
|
XM_011545947.2:c.3132_3133delinsTG
|
XP_011544249.1:p.Thr1044=
|
|
XM_011545948.2:c.2241_2242delinsTG
|
XP_011544250.1:p.Thr747=
|
|
XM_017023671.1:c.3119+7283_3119+7284delinsTG
|
XP_016879160.1:n.3119+7283_3119+7284delinsTG
|
|
XM_017023672.2:c.3113+7283_3113+7284delinsTG
|
XP_016879161.1:n.3113+7283_3113+7284delinsTG
|
|
XM_017023673.2:c.3126_3127delinsTG
|
XP_016879162.1:p.Thr1042=
|
|
NM_024675.4:c.3126_3127delinsTG
MANE Select
|
NP_078951.2:p.Thr1042=
|
|