ENST00000700555.2:n.696T>G
|
|
|
ENST00000700557.2:n.285T>G
|
|
|
ENST00000700559.2:c.2168-3542T>G
|
ENSP00000515065.2:n.2168-3542T>G
|
|
ENST00000546498.2:n.880T>G
|
|
|
ENST00000549461.2:n.685T>G
|
|
|
ENST00000700555.1:c.624T>G
|
ENSP00000515062.1:p.Val208=
|
|
ENST00000700556.1:c.664T>G
|
|
|
ENST00000700557.1:c.204T>G
|
ENSP00000515064.1:p.Val68=
|
|
ENST00000700558.1:n.407T>G
|
|
|
ENST00000700559.1:c.1383-3542T>G
|
|
|
ENST00000700560.1:n.1408T>G
|
|
|
ENST00000700561.1:n.1534T>G
|
|
|
ENST00000070846.11:c.2325T>G
|
ENSP00000070846.6:p.Val775=
|
|
ENST00000340811.9:c.2193T>G
MANE Select
|
ENSP00000342800.5:p.Val731=
|
|
ENST00000070846.10:c.2325T>G
|
ENSP00000070846.6:p.Val775=
|
|
ENST00000340811.8:c.2193T>G
|
ENSP00000342800.4:p.Val731=
|
|
ENST00000613243.1:c.2325T>G
|
ENSP00000478295.1:p.Val775=
|
|
NM_001005242.2:c.2193T>G
|
NP_001005242.2:p.Val731=
|
|
NM_004572.3:c.2325T>G , LRG_398t1:c.2325T>G
|
NP_004563.2:p.Val775=
|
|
NM_001005242.3:c.2193T>G
MANE Select
|
NP_001005242.2:p.Val731=
|
|
NM_004572.4:c.2325T>G
|
NP_004563.2:p.Val775=
|
|