ENST00000561514.3:c.3503_3504delinsGT
|
ENSP00000460666.3:p.Gly1168=
|
|
ENST00000565038.2:c.*982_*983delinsGT
|
ENSP00000459882.2:n.*982_*983delinsGT
|
|
ENST00000566069.6:c.*132_*133delinsGT
|
ENSP00000459237.2:n.*132_*133delinsGT
|
|
ENST00000697377.2:c.3341_3342delinsGT
|
ENSP00000513286.2:p.Gly1114=
|
|
ENST00000697379.2:c.3503_3504delinsGT
|
ENSP00000513287.2:p.Gly1168=
|
|
ENST00000561514.2:c.2612_2613delinsGT
|
ENSP00000460666.2:p.Gly871=
|
|
ENST00000697374.1:c.2612_2613delinsGT
|
ENSP00000513284.1:p.Gly871=
|
|
ENST00000697375.1:n.4844_4845delinsGT
|
|
|
ENST00000697376.1:c.*132_*133delinsGT
|
ENSP00000513285.1:n.*132_*133delinsGT
|
|
ENST00000697377.1:c.2450_2451delinsGT
|
ENSP00000513286.1:p.Gly817=
|
|
ENST00000697378.1:n.4017_4018delinsGT
|
|
|
ENST00000697379.1:c.2612_2613delinsGT
|
ENSP00000513287.1:p.Gly871=
|
|
ENST00000697380.1:n.2701_2702delinsGT
|
|
|
ENST00000697381.1:n.2192_2193delinsGT
|
|
|
ENST00000697382.1:c.*274_*275delinsGT
|
ENSP00000513288.1:n.*274_*275delinsGT
|
|
ENST00000697383.1:c.1031_1032delinsGT
|
ENSP00000513289.1:p.Gly344=
|
|
ENST00000261584.9:c.3497_3498delinsGT
MANE Select
|
ENSP00000261584.4:p.Gly1166=
|
|
ENST00000261584.8:c.3497_3498delinsGT
|
ENSP00000261584.4:p.Gly1166=
|
|
ENST00000566069.5:c.263_264delinsGT
|
|
|
ENST00000568219.5:c.2612_2613delinsGT
|
ENSP00000454703.2:p.Gly871=
|
|
NM_024675.3:c.3497_3498delinsGT , LRG_308t1:c.3497_3498delinsGT
|
NP_078951.2:p.Gly1166=
|
|
XM_011545946.1:c.3503_3504delinsGT
|
XP_011544248.1:p.Gly1168=
|
|
XM_011545947.1:c.*132_*133delinsGT
|
XP_011544249.1:n.*132_*133delinsGT
|
|
XM_011545948.1:c.2612_2613delinsGT
|
XP_011544250.1:p.Gly871=
|
|
XR_950851.1:n.4205_4206delinsGT
|
|
|
XM_011545946.2:c.3503_3504delinsGT
|
XP_011544248.1:p.Gly1168=
|
|
XM_011545947.2:c.*132_*133delinsGT
|
XP_011544249.1:n.*132_*133delinsGT
|
|
XM_011545948.2:c.2612_2613delinsGT
|
XP_011544250.1:p.Gly871=
|
|
XM_017023671.1:c.3266_3267delinsGT
|
XP_016879160.1:p.Gly1089=
|
|
XM_017023672.2:c.3260_3261delinsGT
|
XP_016879161.1:p.Gly1087=
|
|
XM_017023673.2:c.*132_*133delinsGT
|
XP_016879162.1:n.*132_*133delinsGT
|
|
NM_024675.4:c.3497_3498delinsGT
MANE Select
|
NP_078951.2:p.Gly1166=
|
|