ENST00000561514.3:c.-944G>T
|
ENSP00000460666.3:n.-944G>T
|
|
ENST00000566069.6:c.-92G>T
|
ENSP00000459237.2:n.-92G>T
|
|
ENST00000697377.2:c.-331G>T
|
ENSP00000513286.2:n.-331G>T
|
|
ENST00000697379.2:c.-237G>T
|
ENSP00000513287.2:n.-237G>T
|
|
ENST00000561514.2:c.-1835G>T
|
ENSP00000460666.2:n.-1835G>T
|
|
ENST00000697376.1:c.-1147G>T
|
ENSP00000513285.1:n.-1147G>T
|
|
ENST00000697377.1:c.-1222G>T
|
ENSP00000513286.1:n.-1222G>T
|
|
ENST00000697379.1:c.-1128G>T
|
ENSP00000513287.1:n.-1128G>T
|
|
ENST00000697382.1:c.-1886G>T
|
ENSP00000513288.1:n.-1886G>T
|
|
ENST00000697383.1:c.-92G>T
|
ENSP00000513289.1:n.-92G>T
|
|
ENST00000697384.1:n.63G>T
|
|
|
ENST00000261584.9:c.-92G>T
MANE Select
|
ENSP00000261584.4:n.-92G>T
|
|
ENST00000261584.8:c.-92G>T
|
ENSP00000261584.4:n.-92G>T
|
|
ENST00000567003.1:n.53G>T
|
|
|
ENST00000568219.5:c.-960G>T
|
ENSP00000454703.2:n.-960G>T
|
|
NM_024675.3:c.-92G>T , LRG_308t1:c.-92G>T
|
NP_078951.2:n.-92G>T
|
|
XM_011545948.1:c.-1111G>T
|
XP_011544250.1:n.-1111G>T
|
|
XM_011545946.2:c.-944G>T
|
XP_011544248.1:n.-944G>T
|
|
XM_011545947.2:c.-944G>T
|
XP_011544249.1:n.-944G>T
|
|
XM_011545948.2:c.-1111G>T
|
XP_011544250.1:n.-1111G>T
|
|
XM_017023671.1:c.-944G>T
|
XP_016879160.1:n.-944G>T
|
|
XM_017023672.2:c.-92G>T
|
XP_016879161.1:n.-92G>T
|
|
XM_017023673.2:c.-92G>T
|
XP_016879162.1:n.-92G>T
|
|
NM_024675.4:c.-92G>T
MANE Select
|
NP_078951.2:n.-92G>T
|
|