ENST00000324300.10:c.*70G>T
|
ENSP00000315011.5:n.*70G>T
|
|
ENST00000648866.1:c.*70G>T
|
ENSP00000496976.1:n.*70G>T
|
|
ENST00000651419.1:c.*70G>T
MANE Select
|
ENSP00000498969.1:n.*70G>T
|
|
ENST00000324300.9:c.*70G>T
|
ENSP00000315011.5:n.*70G>T
|
|
ENST00000358556.8:c.*70G>T
|
ENSP00000351359.4:n.*70G>T
|
|
ENST00000503721.1:n.894G>T
|
|
|
ENST00000506066.1:c.1027G>T
|
ENSP00000425281.1:n.1027G>T
|
|
ENST00000510697.5:c.1155G>T
|
ENSP00000427259.1:n.1155G>T
|
|
ENST00000511804.5:c.*70G>T
|
ENSP00000425354.1:n.*70G>T
|
|
NM_001166055.1:c.*70G>T
|
NP_001159527.1:n.*70G>T
|
|
NM_001256283.1:c.*70G>T
|
NP_001243212.1:n.*70G>T
|
|
NM_001957.3:c.*70G>T
|
NP_001948.1:n.*70G>T
|
|
NR_045958.1:n.1685G>T
|
|
|
NR_148963.1:n.1394G>T
|
|
|
NR_148964.1:n.1195G>T
|
|
|
NM_001957.4:c.*70G>T
MANE Select
|
NP_001948.1:n.*70G>T
|
|
NR_045958.2:n.1505G>T
|
|
|
NR_148963.2:n.1214G>T
|
|
|
NR_148964.2:n.1015G>T
|
|
|
NM_001166055.2:c.*70G>T
|
NP_001159527.1:n.*70G>T
|
|