|
ENST00000261769.10:c.*2G=
MANE Select
|
ENSP00000261769.4:n.*2G=
|
|
|
ENST00000261769.9:c.*2G=
|
ENSP00000261769.4:n.*2G=
|
|
|
ENST00000422392.6:c.*2G=
|
ENSP00000414946.2:n.*2G=
|
|
|
ENST00000562118.1:n.869G=
|
|
|
|
ENST00000562836.5:n.2722G=
|
|
|
|
ENST00000566510.5:c.*1317G=
|
ENSP00000458139.1:n.*1317G=
|
|
|
ENST00000566612.5:c.*891G=
|
ENSP00000454782.1:n.*891G=
|
|
|
ENST00000611625.4:c.*2G=
|
ENSP00000481063.1:n.*2G=
|
|
|
ENST00000612417.4:c.1854-690G=
|
ENSP00000478360.1:n.1854-690G=
|
|
|
ENST00000621016.4:c.1866-702G=
|
ENSP00000480664.1:n.1866-702G=
|
|
|
NM_004360.3:c.*2G= , LRG_301t1:c.*2G=
|
NP_004351.1:n.*2G=
|
|
|
XM_011523488.1:c.*2G=
|
XP_011521790.1:n.*2G=
|
|
|
XM_011523489.1:c.*2G=
|
XP_011521791.1:n.*2G=
|
|
|
NM_001317184.1:c.*2G=
|
NP_001304113.1:n.*2G=
|
|
|
NM_001317185.1:c.*2G=
|
NP_001304114.1:n.*2G=
|
|
|
NM_001317186.1:c.*2G=
|
NP_001304115.1:n.*2G=
|
|
|
NM_004360.4:c.*2G=
|
NP_004351.1:n.*2G=
|
|
|
NM_004360.5:c.*2G=
MANE Select
|
NP_004351.1:n.*2G=
|
|
|
NM_001317184.2:c.*2G=
|
NP_001304113.1:n.*2G=
|
|
|
NM_001317185.2:c.*2G=
|
NP_001304114.1:n.*2G=
|
|
|
NM_001317186.2:c.*2G=
|
NP_001304115.1:n.*2G=
|
|
