ENST00000399429.8:c.3205+439T>G
MANE Select
|
ENSP00000382356.3:n.3205+439T>G
|
|
ENST00000399429.7:c.3205+439T>G
|
ENSP00000382356.3:n.3205+439T>G
|
|
ENST00000430711.5:c.256+439T>G
|
ENSP00000413093.1:n.256+439T>G
|
|
ENST00000453441.1:c.70+439T>G
|
ENSP00000391380.1:n.70+439T>G
|
|
NM_001037763.2:c.3205+439T>G
|
NP_001032852.2:n.3205+439T>G
|
|
XM_011515358.1:c.3205+439T>G
|
XP_011513660.1:n.3205+439T>G
|
|
XM_011515359.1:c.3205+439T>G
|
XP_011513661.1:n.3205+439T>G
|
|
XM_011515360.1:c.3205+439T>G
|
XP_011513662.1:n.3205+439T>G
|
|
XM_011515362.1:c.2056+439T>G
|
XP_011513664.1:n.2056+439T>G
|
|
XR_926936.1:n.3408+439T>G
|
|
|
XM_011515358.3:c.3205+439T>G
|
XP_011513660.1:n.3205+439T>G
|
|
XM_011515359.2:c.3205+439T>G
|
XP_011513661.1:n.3205+439T>G
|
|
XM_011515360.2:c.3205+439T>G
|
XP_011513662.1:n.3205+439T>G
|
|
XM_011515362.2:c.2056+439T>G
|
XP_011513664.1:n.2056+439T>G
|
|
XM_017012131.2:c.3205+439T>G
|
XP_016867620.1:n.3205+439T>G
|
|
XM_017012132.2:c.3205+439T>G
|
XP_016867621.1:n.3205+439T>G
|
|
XR_001744688.1:n.4831+439T>G
|
|
|
XR_926936.3:n.4607+439T>G
|
|
|
NM_001037763.3:c.3205+439T>G
MANE Select
|
NP_001032852.2:n.3205+439T>G
|
|