|
ENST00000261769.10:c.*47G=
MANE Select
|
ENSP00000261769.4:n.*47G=
|
|
|
ENST00000261769.9:c.*47G=
|
ENSP00000261769.4:n.*47G=
|
|
|
ENST00000562118.1:n.914G=
|
|
|
|
ENST00000566612.5:c.*936G=
|
ENSP00000454782.1:n.*936G=
|
|
|
ENST00000611625.4:c.*47G=
|
ENSP00000481063.1:n.*47G=
|
|
|
ENST00000612417.4:c.1854-645G=
|
ENSP00000478360.1:n.1854-645G=
|
|
|
ENST00000621016.4:c.1866-657G=
|
ENSP00000480664.1:n.1866-657G=
|
|
|
NM_004360.3:c.*47G= , LRG_301t1:c.*47G=
|
NP_004351.1:n.*47G=
|
|
|
XM_011523488.1:c.*47G=
|
XP_011521790.1:n.*47G=
|
|
|
XM_011523489.1:c.*47G=
|
XP_011521791.1:n.*47G=
|
|
|
NM_001317184.1:c.*47G=
|
NP_001304113.1:n.*47G=
|
|
|
NM_001317185.1:c.*47G=
|
NP_001304114.1:n.*47G=
|
|
|
NM_001317186.1:c.*47G=
|
NP_001304115.1:n.*47G=
|
|
|
NM_004360.4:c.*47G=
|
NP_004351.1:n.*47G=
|
|
|
NM_004360.5:c.*47G=
MANE Select
|
NP_004351.1:n.*47G=
|
|
|
NM_001317184.2:c.*47G=
|
NP_001304113.1:n.*47G=
|
|
|
NM_001317185.2:c.*47G=
|
NP_001304114.1:n.*47G=
|
|
|
NM_001317186.2:c.*47G=
|
NP_001304115.1:n.*47G=
|
|
